Open access peer-reviewed chapter

Optical Sensing (Nano)Materials Based on Benzimidazole Derivatives

Written By

Ema Horak, Robert Vianello and Ivana Murković Steinberg

Submitted: December 3rd, 2018 Reviewed: March 5th, 2019 Published: April 3rd, 2019

DOI: 10.5772/intechopen.85643

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Abstract

Benzimidazole derivatives are well-known biologically active substances, and therefore, they are mostly synthesised for therapeutic purposes. However, such heteroaromatic molecular systems own structure-related properties that enable a variety of applications, especially in optical science. Multifunctionality of the benzimidazole unit, such as electron accepting ability, π-bridging, chromogenic pH sensitivity/switching and metal-ion chelating properties, makes it an exceptional structural candidate for the design of optical chemical sensors and functional materials. Development of smart molecular sensors and novel (nano)materials is the emerging trend observed in materials and optical sensing science in general, in which the benzimidazole molecular systems strongly contribute and participate. In this chapter, we summarised recent advances in optical sensing (nano)materials that incorporate the benzimidazole structural moiety. Solid-state optical sensing systems, including self-assembled molecular materials based on benzimidazoles, are reviewed and discussed. In addition, immobilisation of benzimidazole derivatives onto or into various substrates and matrices, such as organic and inorganic polymers, bulk membranes and nanoparticles, utilising different chemical and physical methods, is presented and analysed.

Keywords

  • benzimidazole
  • functional materials
  • optical sensor
  • solid-state
  • absorbance
  • fluorescence
  • aggregation-induced emission

1. Introduction

Optical chemical sensors are widely applied in chemical science and technology, as well as in other disciplines such as biology, medicine and environmental science. They enable continuous monitoring of the target analytes and exhibit high sensitivity and fast response time. The biggest advantages of optical chemical sensors, in comparison to other sensing devices, are the economic production, ease of operation and the possibility of on-site application without reference devices, which are preferred in chemical and biological applications. Performance of every chemical sensor is primarily determined by the sensing chemistry that operates in the background, that is, the recognition unit—receptor. The receptor, the core of every optical chemical sensor, is the sensing molecule that selectively responses to the presence of the target analyte by changing the photophysical properties of the observed molecular system. Fluorescence techniques are most commonly applied for the generation and transfer of the analytical signal, while providing high sensitivity and selectivity. Therefore, fluorescent sensing molecules are the most promising candidates for the chemical sensing. Their design often starts from the heterocyclic molecular skeleton, due to its excellent spectral properties and the ability to detect diverse analytes. Heterocyclic chromophores and fluorophores are the most investigated classes of optical sensing molecules; hence, the interest for benzimidazole as a structural block of novel molecular systems is constantly increasing. Although benzimidazole derivatives are primarily known as biologically and therapeutically active substances [1], such heteroaromatic molecules have structure-related properties that enable a variety of applications in optoelectronics and non-linear optics (NLO) [2, 3], photovoltaics [4, 5], sensing [6] and bioimaging [7, 8]. Indeed, multifunctionality of the benzimidazole unit, such as electron accepting ability, π-bridging, chromogenic pH sensitivity/switching and metal-ion chelating properties, makes it an exceptional structural candidate for the design of optical chemical sensors [9, 10]. From the chemical point of view, the benzimidazole ring possesses a high degree of stability. Benzimidazole, for example, is not affected by concentrated sulphuric acid and is quite resistant to reduction. Oxidation cleaves its benzene ring, yet only under vigorous conditions. The two imidazole nitrogens are different from one another in their nature, which makes the properties of the ring system diverse in character. The hydrogen attached to the nitrogen can easily tautomerise to the other nitrogen atom. With the pKa values 5.3 and 12.3, benzimidazoles are weakly basic, being somewhat less basic than the imidazoles and sufficiently acidic to make them usually more soluble in polar environments and less soluble in organic solvents. Benzimidazole, for example, is soluble in hot water but difficultly soluble in ether and insoluble in benzene, all of which can be modified upon the substitution. The acid/base properties of benzimidazoles are due to the stabilisation of the charged ion by the resonance effect.

However, development of optical chemical sensors is much more complicated than designing a sensing molecule (recognition unit), since the process combines molecular recognition, material science and device implementation. Employing the sensing chemistry in a form of optical sensing material is perhaps the key step towards the ultimate goal, since its implementation can directly result in a functional sensor. Although there is a large number of fluorescent indicators and sensing molecules presented in literature, many of them lose their selectivity upon the implementation in functional devices, which makes the design of optical sensing materials a very challenging task [11, 12].

Recently, developments in optical sensing molecular systems that incorporate benzimidazole structural unit are reviewed and discussed [13]. As can be deduced from a given review, molecular sensors based on benzimidazole derivatives are mainly applied in solution, while materials for optical sensing are still rare, yet very promising. Development of novel (nano)materials and especially ‘smart’ molecular sensors, some of which include nanotubes, nanowires and nanoparticles, is the emerging trend observed in materials and optical sensing science. Although the growth of scientific interest in benzimidazole-based materials is evident in the last decade, such systems are indeed untapped potential in the field of optical chemical sensing.

In this chapter, we summarised the recent advances in optical solid state sensing systems and (nano)materials that incorporate the benzimidazole structural moiety. Immobilisation of benzimidazole derivatives in bulk membranes, polymers, sol-gel materials, as well as self-assembled (nano)materials for optical sensing are reviewed and discussed. Representative examples have been selected and commented in next sections, based on the type of applied material.

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2. Polymer-based sensing materials

Polymers are the most commonly used support for optical chemical sensors [14]. They can be utilised to immobilise the sensing component, but can also directly participate in the sensing mechanism. In general, most commonly used polymers for analyte sensing are cellulose derivatives and hydrogels because of their excellent mechanical properties, stability at broad temperature and pH ranges, as well as high permeability towards water, ions and undissolved gases. In addition, polymers like polyurethane and pHEMA are biocompatible, a fact that enables new possibilities of their application.

The simplest form of the polymeric sensing material is the polymer membrane in which the chemosensor molecule is physically entrapped [11, 12]. Such dye-impregnated polymers are widely used in sensing chemistry, due to economic and simple methods of preparation. The choice of polymer depends on its permeability towards a specific analyte, its stability, availability and potential for immobilisation. Still, the development of such membranes is a challenging task because the polymer microenvironment has a strong effect on spectral characteristics of the immobilised sensing molecule, its acid-base equilibrium, selectivity towards the analyte and fluorescence lifetime. Ion-selective optodes are well-known examples of such optical sensing systems, where the bulk membranes are mostly formed from plasticised PVC [15].

An alternative for dye-impregnated polymers are the polymers with covalently attached fluorescent molecules. Stability of covalently bonded systems provides many advantages and can significantly improve analytical performance of chemical sensor. Another class of materials for optical sensing is the luminescent polymers. Design and synthesis of novel conjugated or coordination polymers is a constantly growing area of research, due to the enormous potential for the application of these kinds of functional materials.

The polymer-based materials for optical sensing that incorporate benzimidazole unit are summarised in Table 1, while the representative examples have been selected and discussed in next sections.

Material Analyte BI-based sensing molecule Detection method Limit of detection (mol L−1) Ref.
PVC Hg2+ Crown-based ionophore Fluorimetric 3.5 × 10−13 Firooz et al. [18]
PVC Ag+ Crown-based ionophore Fluorimetric 2.8 × 10−12 Firooz et al. [19]
PVC pH Acrylonitrile derivative Colorimetric Horak et al. [20]
PVC pH Schiff bases Fluorimetric Horak et al. [21]
Photocrosslinked membrane Hg2+ 1,8-naphthalimide derivative Fluorimetric 2.5 × 10 −6 Fernández-Alonso et al. [22]
Amphiphilic copolymer pH Vinyl monomer Fluorimetric Han et al. [29]
Hydrophilic copolymer pH Pyridyl substituted benzimidazole derivative Fluorimetric Shen et al. [30]
Conjugated polymer Cu2+ Pendant benzimidazolyl moieties Fluorimetric Wu et al. [28]
Conjugated polymer Fe3+ and PO43− Pendant benzimidazolyl moieties Fluorimetric 3.38 × 10−6 Saikia et al (2011) [27]
Coordination polymer Fe3+ Bis(benzimidazole) derivative Fluorimetric 3.2 × 10−6 Hao et al. [36]
Metal organic framework Humidity and formaldehyde Benzimidazolyl-attached bent organic ligand Colorimetric Yu et al. (2014) [32]
Metal organic framework Cr2O72− 1,6-Bis(benzimidazol-1-yl)hexane ligand Fluorimetric 2.16 × 10−6 Li et al. [31]
Coordination polymer Fe3+ ion and nitroaromatics Benzimidazole ligand Fluorimetric 3.70 × 10−7 Zhou et al. [33]
Coordination polymer Multi-analyte Benzimidazole-appended tripodal tridentate ligand Fluorimetric Tripathi et al. [37]
Coordination polymer pH Benzimidazole-functionalized organic ligand Phosphorescence Yang et al. [38]
Coordination polymer Fe3+ Benzimidazole-functionalized organic ligand Fluorimetric 2.53 × 10−6 Zhao et al. [39]
Coordination polymer Fe3+ Benzimidazole-functionalized organic ligand Fluorimetric 2.72 × 10−5 Wei et al. [40]
Zr-UiO-66 nanocrystals Fe3+ Benzimidazole-functionalized organic ligand Fluorimetric Dong et al. [34]

Table 1.

Polymeric optical sensing materials based on benzimidazole derivatives.

2.1 Dye-impregnated polymers

Polymer-based sensing materials incorporating physically entrapped benzimidazole-based receptors are very often used when relying on the electrochemical detection [16, 17]. However, examples utilising optical sensing techniques are not that common. For example, novel fluorescent sensors are developed by the immobilisation of benzimidazole-based ionophores in plasticised PVC, resulting in ion-selective optode for mercury [18] and silver detection [19]. Presented ion-selective optodes are complex systems, where a number of parameters, including lipophilicity, polarity and microviscosity affect the heterogeneous ion-exchange equilibrium. The same sensing mechanism is presented for benzimidazole-based acrylonitrile derivatives [20] and Schiff bases [21], where novel colorimetric and fluorimetric sensing materials are applied for detecting the acidity changes. Moreover, immobilisation of this class of compounds into polymer matrices is demonstrated as a convenient way to overcome certain problems of organic fluorophores occurring in aqueous solution, such as hydrolysis of imino-bond or low quantum yields. For instance, a reversible spectroscopic response to pH is achieved because protonation of the immobilised benzimidazole Schiff bases occurs on the stable benzimidazole moiety (electron acceptor), while the imino bond of the Schiff base remains preserved [21]. At the same time, spectral properties of fluorescent sensing molecules are significantly altered due to the interactions between molecules in bulk, that is, in novel environment, where the molecular system becomes more rigid with partially disabled cis-trans isomerisation. Optical properties of developed materials can also be easily modified by tuning the ICT character of fluorescent molecules, which is often achieved by introducing electron donating groups (e.g. N,N-diethyl amino) and strong electron withdrawing moieties (e.g. -CN and –NO2) on the opposite parts of molecular system (Figure 1A).

Figure 1.

(A) Fluorescent pH-sensitive bulk optodes based on immobilised Schiff base derivatives in plasticised PVC matrix. Tuneable fluorescent response of the optodes is a result of different substituents on the benzimidazole moiety. Reprinted from [21]. Copyright (2018), with permission from Elsevier. (B) Selective fluorescence solid sensor for Hg2+ based on N-(2-hydroxyethyl)-4-(4-(1Hbenzo[d]imidazol-2-yl)methyl) piperazine-1-yl)-1,8-naphthalimide, here presented by the author's courtesy. Fluorescence sensor undergoes fluorescence enhancement upon binding mercuric ion due to the inhibition of photo-induced electron transfer (PET) process from the piperazine to the naphthalimide moiety [22].

2.2 Covalently attached benzimidazole derivatives

As an alternative to dye-impregnation of polymers, fluorescent molecules can be covalently attached to polymeric materials, as demonstrated, for example, in a fluorescence solid sensor for the mercury detection based on a photocrosslinked membrane functionalised with (benzimidazolyl)methyl-piperazine derivative of 1,8-naphthalimide [22]. Benzimidazole, linked to a piperazine moiety by a methylene spacer, is responsible for the specific recognition of Hg2+ ions by forming a stable complex structure, that resulted in a strong fluorescence (Figure 1B). Materials developed by the covalent attachment of the sensing molecules usually have more advantages that those utilising physical entrapment, in which active molecules may easily leach out of the matrix. Stability and duration of covalently functionalised polymer materials are much better, and they even often provide improved analytical parameters of chemical sensor.

2.3 Luminescent polymers

Another approach to obtain fluorescent sensing materials is a clever design and synthesis of novel luminescent polymers. For instance, conjugated polymers are the constant trend in the development of novel functional materials [23, 24]. They effectively coordinate with many organic compounds or transition metals, which is very well conjoined with their excellent optical properties and exploited in optical chemical sensors. Detection methods are mostly relying on the fluorescence techniques, particularly the quenching effect (‘superquenching’) described by Stern-Volmer relationships. Fluorescent conjugated polymers also offer many advantages in regard to simple organic fluorophores, such as amplified sensitivity and the possibility of simple introduction of desired functional groups in order to achieve better interactions with the analyte. Benzimidazole is often found as a constituent of conjugated polymers [25, 26, 27, 28]. Optical sensing ability of benzimidazole-based fluorescent polymers is demonstrated for the detection of pH [29, 30], metal ions [28] or inorganic anions [27], where benzimidazole moiety often plays a crucial role in the sensing mechanism. For example, a copolymer built from N-(1-ethyl-2-(pyridin-4-yl)-1Hbenzo[d]imidazol-5-yl)methacrylamide and 2-hydroxyethyl methacrylate exhibits a pH sensitivity due to acid-base equilibria on the heteroatom of pyridyl-substituted benzimidazole moiety [30] (Figure 2A).

Figure 2.

(A) Chemical structure of pH-responsive copolymer of N-(1-ethyl-2-(pyridin-4-yl)-1Hbenzo[d]imidazol-5-yl) methacrylamide and 2-hydroxyethyl methacrylate, here presented by the author's courtesy. pH sensitivity is achieved by pyridyl substituted benzimidazole moiety [30]. (B) Representation of multistimuli-responsive ‘smart’ mercury(II) coordination polymer and different possible conformations of benzimidazole-based ligand in metal complexes. Adapted with permission from [37]. Copyright (2018) American Chemical Society.

Besides conjugated polymers, benzimidazole-based materials can be developed as luminescent metal organic frameworks (MOFs) [31, 32, 33, 34, 35] or coordination polymers [36, 37, 38, 39, 40, 41, 42]. Such advanced functional materials have been extensively applied in the field of luminescence sensing due to their diverse structural characteristics and tunable pore sizes. For example, luminescence sensing of iron is achieved by a coordination polymer employing the linear 2,5-dichloroterephthalic acid ligand and the flexible bis(benzimidazole) derivatives. Ligand affords the capacity to strongly bind metal atoms, while bis(benzimidazole) derivatives can freely twist around two methylene -CH2 groups with disparate angles to generate different conformations [36]. Luminescent MOFs have been exploited for the development of sensing materials for humidity and formaldehyde, such as a porous Cu(I)-MOF, constructed from CuI and 1-benzimidazolyl-3,5-bis(4-pyridyl)benzene (Figure 3) [32]. 3D cadmium metal-organic framework was demonstrated as sensing material for the detection of Cr2O72− in water [31], while diamond-like coordination polymer exhibits selective emission quenching responses towards the Fe3+ ion and nitroaromatics [33].

Figure 3.

(A) Highly sensitive naked eye colorimetric sensor for water and formaldehyde detection based on a porous Cu(I)-MOF constructed from CuI and 1-benzimidazolyl-3,5-bis(4-pyridyl)benzene. (B) The colour change of the bulk crystal samples of MOF in atmospheres with different relative humidity (RH 33–78.5%) and the corresponding solid-state emission spectra. Adapted with permission from [32]. Copyright (2013) Royal Society of Chemistry.

Interesting to note is the emerging trend in the development of the so-called ‘smart’ materials, where the final product exhibit multistimuli-responsive photoluminescence sensing properties. Tripathi et al. developed Hg(II) coordination polymer with benzimidazole-appended tripodal tridentate ligand, 1,3,5-tris(benzimidazolylmethyl)benzene. Luminescent material is the first example of Hg(II) coordination polymer with multistimuli-responsive properties (Figure 2B). Luminescence quenching response is observed to a range of stimuli, including anions, solvents and nitroaromatic compounds [37].

2.4 Inorganic polymers

Inorganic polymers, such as networks of metal oxides obtained by sol-gel process, are also attractive substrates for immobilising sensing molecules. Sol-gel materials are very popular for the development of optical sensors, especially nanosized probes [43]. Basically, the sol-gel process is a method for the synthesis of ceramic or glass materials at low temperature, starting from the colloidal suspension (‘sol’). Hydrolysis of alkoxy metal groups in the precursors followed by polycondensation results in a network structure (‘gel’). Meantime, fluorescent indicators can be easily incorporated in sol-gel by impregnation, chemical or covalent immobilisation. These materials are porous, so that the analyte can freely diffuse. They are robust and biocompatible, which makes them suitable for intracellular sensing. Hoffman et al. have developed novel benzimidazole-based fluorescent materials using the sol-gel process [44]. Tetraethylorthosilicate (TEOS) was used as an inorganic precursor for the development of new silica hybrid materials. Although sol-gel chemistry is firmly embedded in the field of chemical sensors, there is a lack of benzimidazole-based sol-gel materials. The reason can be poor solubility and self-assembly properties of many benzimidazole derivatives, often inducing gelation process and thus, making the development of novel sol-gel materials, in a classical manner described above, a challenging task. However, the gelation of such compounds has been shown as an excellent method for preparing new sensing membranes, which will be discussed in further sections.

To conclude this section, we can highlight several facts. Literature shows that polymer-based materials are the most common substrates for the preparation of novel optical sensing platforms based on benzimidazole derivatives. Benzimidazole moiety retained its functional properties upon immobilisation in presented polymeric platforms. Although they are thoroughly explored and their potential for sensing applications is often emphasised, luminescent polymers that incorporate benzimidazole moiety are not adequately exploited in optical sensors. Even though polymer-based sensing materials are still relatively rare, a recent advance in developing benzimidazole-based ultralong-persistent room temperature phosphorescence (RTP) materials that exhibit reversible pH-responsive emission [38] represents a significant breakthrough of benzimidazole derivatives in materials science. Unfortunately, the biggest disadvantages of most polymer-based sensing materials are still very limited, such as selectivity, poor photostability and often leaching of indicator dyes.

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3. Self-assembled sensing materials

3.1 Gels

Soft matter research and supramolecular organogels are one of the emerging scientific areas in the last decade. Functional materials based on supramolecular organogels are very attractive for the applications in tissue engineering, medical implants, controlled drug release, environmental studies etc. Small organic molecules have often been investigated as π-gelators, including benzimidazole derivatives [46, 47]. Utilising their fluorescence and self-assembling properties, benzimidazole-based gels are successfully demonstrated as novel functional materials. For example, a family of alkylpyridinylium benzimidazole derivatives was synthesised in order to examine its gelation properties [48], while several fluorescent π-gelators based on benzimidazole are presented as stimuli responsive systems and sensors [49, 50, 51, 52, 53]. Ghosh et al. presented sensing system for Ag+ based on the cholesterol-appended benzimidazole. Benzimidazole moiety with conformational flexibility can exhibit different alignments upon metal ion chelation, while the cholesterol is likely oriented to exert hydrophobic-hydrophobic interaction for establishing cross-linked network for solvent trapping. The addition of Ag+ ions to the solution of presented molecules in DMF:H2O (1:1, v/v) at room temperature causes instant gelation and the change of colour, visible by a naked eye [51]. Another example of multi-analyte sensor array based on benzimidazole and acylhydrazone naphthol moities was demonstrated by Yao et al. [52]. The latter sensing system is able to detect many analytes such as CN, Al3+, Fe3+ and L-Cys with a possibility for the selective identification of Fe3+ and Al3+ in the gel state (Figure 6).

3.2 Aggregation-induced emitters

Self-assembly of benzimidazole derivatives takes a great role in emerging mechanisms and designs of novel optical sensing materials. One of the research directions of the self-assembled molecules are the sensing materials based on the emissive (nano)aggregates. Aggregation of organic fluorophores is mostly investigated as an undesirable side effect in many biological or chemical applications due to fluorescence quenching. However, development of novel organic luminophores with aggregation-induced emission (AIE) changed the aspect of aggregation phenomena and the AIE was introduced as an analytical tool in a wide range of application, such as bioimaging, optoelectronics and chemosensors [54]. AIE or AIEE (aggregation-induced emission enhancement) can be observed in the so called ‘poor’ solvents, in crystalline or powder forms. With that in mind, benzimidazole-based fluorophores capable of emitting intense fluorescence in the aggregated form (AIE emitters) can also be classified as novel sensing materials [55, 56, 57, 58]. For example, self-assembled nanoaggregates of benzimidazole-based acrylonitrile derivative are presented as sensing system for pH, based on aggregation-deaggregation mechanism and aggregation-induced emission (AIE) [59]. 2-Benzimidazolyl-substituted acrylonitrile dye exhibits fluorescence emission in the red, green or cyan spectral regions, depending on its protonation degree. The neutral form is capable of self-assembly in the aqueous environment (pH between 5 and 9), exhibiting stable red-orange fluorescence emission at 600 nm. Thus, due to the aggregation-induced emission (AIE), from the single molecular entity, tri-state system (RGB) is derived. The aggregation and emission are pH switchable and fully-reversible. Gogoi et al. presented a novel AIE system based on a benzimidazole derivative for the detection of pyrophosphate (PPi) (Figure 4) [56]. The benzimidazole moiety has a functional role in assembling aggregate structures and the recognition of Ppi. Molecules of benzimidazole derivative self-assemble in nanostructures when so-called ‘bad’ solvent, H2O, is added into the THF solution (‘good’ solvent). Self-assembled nanostructures exhibit pronounced emission at λ = 530 nm. Their π-π stacking is affected by the Ppi presence, thus assembled aggregates are of different emission properties and sizes. Another example is offered by Singh et al. by the preparation of fluorescent aggregates for sensing chemical warfare agents (diethylchlorophosphate) from benzimidazolium-based receptors containing 2-mercaptobenzimidazole and 2-mercaptobenzthiazole as functional groups, using anionic surfactants [60]. Authors presented receptors with benzimidazolium moiety in the centre, as well as receptors with two fluorescent arms as binding- and signalling units that initially interacts with chemical warfare agents and captures the hydrolysed product of an organophosphate.

Figure 4.

Aggregation-induced emission of benzimidazole-based derivative and detection of pyrophosphate (PPi). Reprinted with permission from [56]. Copyright (2015) American Chemical Society.

An AIE phenomenon is especially exploited in solid-state, where the concentration effect commonly causes fluorescence quenching. Having in mind that fluorophores emitting in the solid states are extremely rare, especially red ones, benzimidazole-based AIE molecular systems show a great prospect for future applications of pristine powder samples or crystals as solid-state sensors and ‘smart’ materials [61, 62, 63, 64, 65].

In conclusion, due to its emerging and multidisciplinary character, further research on optical sensing applications of benzimidazole-based gel membranes and self-assembled structures is strongly encouraged. Gelation is proven and widely investigated effect in many benzimidazole-based compounds, yet not exploited enough for the preparation of novel chemical sensors. Meanwhile, research on the aggregation-induced emission phenomena has taken momentum in all areas of application. Beside the fact that certain benzimidazole-based derivatives exhibit AIE property, which is not often found within small heterocyclic molecular systems, optical chemical sensors based on this principle are rarely found. Self-assembled materials for optical sensing that incorporate benzimidazole unit are summarised in Table 2.

Material Analyte BI-based sensing molecule Detection method Limit of detection (mol L−1) Ref.
Gel Multi-analyte Benzimidazole and acylhydrazone naphthol moities Fluorimetric Yao et al. [52]
Gel Ag+ Cholesterol appended benzimidazole Colorimetric 4.31 × 10−5 Ghosh et al. [51]
Gel pH and anions Benzimidazole moiety and four amide units Colorimetric /Fluorimetric Xue et al. [49]
Gel Picric acid Cholesterol-based anthraquinone-coupled imidazole Colorimetric 4.30 × 10−6 Mondal et al. [50]
Gel Na2S Carboxylic acid functionalized benzimidazole Fluorimetric Yao et al. [53]
AIEgen Pyrophosphate Dipodal benzimidazole- functionalized sensor Fluorimetric 1.67 × 10−9 Gogoi et al. [56]
AIEgen pH Acrylonitrile derivative Fluorimetric Horak et al. [59]
AIEgen Warfare agents Benzimidazolium-based dipodal receptors Fluorimetric 10 × 10−9 Singh et al. [60]
Powder F and COO Benzimidazole derivative Colorimetric 0.38 × 10−3 Chaudhuri et al. [64]
SBA-15 nanoporous silica Hg2+ 2,6-bis(2-benzimidazolyl) derivative Fluorimetric 2.6 × 10−6 Badiei et al. [71]
ZnO nanoparticles Zn2+ Benzimidazole-based organic ligand Colorimetric 4.09 × 10−9 Kaur et al. [72]
Nano hyperbranched polyester Fe3+ Benzimidazole end groups Fluorimetric Wang et al. [73]
Filter paper TNT Pyrene-substituted benzimidazole-isoquinolinones Colorimetric 50 × 10−6 Boonsri et al. [74]
Filter paper CN Acrylonitrile-embedded benzimidazole-anthraquinone Colorimetric 37 × 10−9 Kumar et al. [76]
Filter paper Ni2+ 2-(2′-hydroxyphenyl)benzimidazole Colorimetric Dhaka et al. [77]
TLC plates Acid/amine vapours Carbazole-based benzimidazole derivatives Colorimetric Aich et al. [75]

Table 2.

Benzimidazole-based materials for optical sensing.

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4. Nanomaterials for optical sensing

Nowadays, the term nano appears in all aspects of our life, technology and science, including the optical chemical sensors. In most general way, an optical nanosensor can be defined as a device smaller than 1 μm that is continuously tracking an analyte and simultaneously converting optical information into an analytically useful signal [66]. Fluorescence is the most commonly applied detection technique, due to its high sensitivity and relative simplicity of measurement [67]. Nanosensors can be macromolecular nanostructures, nano-sized polymer materials and sol-gels, multi-functional core-shell systems, multi-functional magnetic beads or nanosensors based on quantum dots or metal beads. We have previously mentioned the nanoaggregates formed by the self-assembly process. Although such type of nanomaterial can be classified as nanosensors, the emphasis in this section is placed on synthesis of nano-sized substrate materials functionalised with benzimidazole derivatives. Most commonly used method for the preparation of nanosensors is previously mentioned sol-gel process resulting in silica nanoparticles [68, 69]. Some other methods, such as precipitation, are often utilised for the preparation of polymer nanoparticles [70]. Research in the field of benzimidazole-based nanosensors is still in the early stages. Benzimidazole-based nanomaterials for optical sensing of metal ions are so far demonstrated as hybrid silica materials [44, 68, 71], ZnO nanoparticles decorated with benzimidazole-based organic ligand [72] or self-assembled nano hyperbranched polymer [73]. For example, Badiei et al. recently presented SBA-15 nanoporous silica functionalised with 2,6-bis(2-benzimidazolyl) pyridine for the selective recognition of mercury (Figure 5) [71]. Fluorescence intensity of the SBA-15 functionalized material quenched in the presence of Hg2+ ions, wherein the sensor is applicable in the physiological pH range of 6–8.

Figure 5.

Synthesis procedure of benzimidazole functionalized SBA-15 material and fluorescence emission of the aqueous suspended nanoparticles (0.4 g L−1) upon titration of increasing amount of Hg2+ ions. Inset: Stern-Volmer plot, λexc = 353 nm. Reprinted with permission from [71]. Copyright (2018) Springer Nature.

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5. Other benzimidazole-based materials for optical sensing

A simple, fast and economic determination of target analyte, on-site and without a reference device is one of the key challenges of modern analytical chemistry. As mentioned in previous sections, the response to this challenge came forth in the form of optical chemical sensors. In addition, design and development of sensing materials as straightforward optical sensors enable countless possibilities of their applications, especially in modern technology where the emphasis is put on mobile, wearable and wireless devices. Simple, yet effective materials for colorimetric or fluorimetric detection of analytes can easily be achieved using filter paper or TLC plates. Paper substrates themselves are an attractive platform for the use in a wide range of optical sensing, due to the possibility of a passive sample manipulation by capillary forces. So far, paper-based optical chemical sensors for neutral molecules, anions and cations, relying on benzimidazole derivatives as recognition element, have been successfully presented by several research groups. For example, Boonsri et al. demonstrated paper-based sensors for the trinitrotoluene (TNT) detection [74]. Sensing material prepared from pyrene-substituted benzimidazole-isoquinolinones can readily detect TNT in aqueous media by a naked-eye observation at concentrations as low as 50 μM. Optical sensing of acid/amine vapours with three carbazole-based benzimidazole derivatives in the solid state was also demonstrated using TLC plates [75]. Plates were immersed with benzimidazole-based dyes and then exposed to trifluoroacetic acid (TFA) vapours for 1 minute. In following step, the TLC plates which were exposed with TFA vapours were further revealed to triethyl amine vapours and the restored colour was observed in each case (Figure 6).

Figure 6.

(A) Proposed self-assembly mechanism of a supramolecular AIE gel and its multiple-stimuli responsive behaviour (a) and fluorescence responses of the multi-analyte sensor array to the presence of various anions, cations and amino acids. Reprinted with permission from [52]. Copyright (2018) Royal Society of Chemistry. (B) TLC plates immersed with carbazole benzimidazole-based dyes observed under the UV light (λexc = 365 nm) before (a) and after exposure to TFA vapours (b). Adapted with permission from [75]. Copyright (2016) Royal Society of Chemistry.

Anion detection was demonstrated by the ratiometric detection of CN based on acrylonitrile embedded benzimidazole-anthraquinone coated on the filter paper [76]. Paper strips coated with the sensing molecule showed a distinct colour change from yellow-greenish to red under UV light in the presence of the CN ions. Dhaka et al. demonstrated a ‘bare-eye’ probe for the detection of Ni2+ based on 2-(2′-hydroxyphenyl)benzimidazole. Colourimetric sensing of Ni2+ was demonstrated on filter paper. Paper test strips exhibit distinct visual change from colourless to yellow-gold [77]. Other materials for optical sensing that incorporate benzimidazole unit are summarised in Table 2.

Besides optical sensing, paper-based materials coated with functional benzimidazole derivatives are also presented as ‘smart’, stimuli responsive materials with potential applications in security, optoelectronic or fluorescent imaging [62]. Simple sensing substrates such as paper and textile materials are perfectly suited for applications in emerging mobile and wearable chemical sensors. Design and development of compatible ‘sensing chemistries’ that operate in the background of such devices is a constant challenge. The multifunctional nature of materials based on molecules such as benzimidazole can perfectly respond to this challenge.

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6. Conclusion

Benzimidazole unit represents an important multifunctional building block in optical chemical sensors, with proven potential for the development of novel functional (nano)materials. Solid-state optical sensing systems incorporating benzimidazole derivatives are reviewed and discussed. Polymers are most commonly used substrates for the development of optical chemical sensors. Materials for optical sensing based on benzimidazole are also demonstrated as gels, sol-gel matrices, silica or polymer nanoparticles, (nano)aggregates and TLC or paper-based strips.

The role of benzimidazole moiety in optical sensing (nano)materials is important and crucial, since it maintains the function of the system and plays a key role in the formation of the analytical signal in the majority of chemical sensing systems reviewed here. Besides, the planar moiety significantly contributes to the conjugation of the chromo/fluorophore system. Although benzimidazole derivatives reviewed in the literature are mostly fluorescent sensors, several probes based on colourimetric switches are also demonstrated. It is very challenging to transfer the sensing chemistry from a solution to the solid state, which is successfully comprehended for the benzimidazole derivatives. It is even observed for some classes of chromophores with relatively unattractive sensing properties in aqueous solution (such as low quantum yield, decomposition upon protonation) to be drastically improved upon immobilisation in a polymer matrix.

Although examples of sensing materials presented in the literature show that benzimidazole derivatives can be successfully and easily applied in optical chemical sensors, they are yet insufficiently explored. Challenges in development of novel optical sensing (nano)materials are constantly emerging, since the scientific and industrial field of mobile and wearable sensors are experiencing great progress. Simple, fast and economic determination of target analyte, on-site and without reference device is a request that a multifunctional molecule such as benzimidazole can perfectly respond to.

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Acknowledgments

This work was supported by the Croatian Science Foundation under grant number IP-2014-09-3386 entitled ‘Design and synthesis of novel nitrogen-containing heterocyclic fluorophores and fluorescent nanomaterials for pH and metal-ion sensing’ which is gratefully acknowledged.

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Conflict of interest

Authors have no conflict of interest to declare.

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AIEaggregation-induced emission
AIEEaggregation-induced emission enhancement
DMFdimethylformamide
ICTintramolecular charge transfer
MOFmetal organic framework
NLOnon-linear optics
pHEMApoly(2-hydroxyethyl methacrylate)
PPipyrophosphate
PVCpoly(vinyl chloride)
RGBred, green and cyan spectrum
RTPultralong-persistent room temperature phosphorescence
SBA-15porous silica
TEOStetraethylorthosilicate
TFAtrifluoroacetic acid
THFtetrahydrofuran
TLCthin layer chromatography
TNTtrinitrotoluene
UVultraviolet

References

  1. 1. Keri RS, Hiremathad A, Budagumpi S, Nagaraja BM. Comprehensive review in current developments of benzimidazole-based medicinal chemistry. Chemical Biology and Drug Design. 2015;86(1):799-845
  2. 2. Hung WY, Chi LC, Chen WJ, Chen YM, Chou SH, Wong KT. A new benzimidazole/carbazole hybrid bipolar material for highly efficient deep-blue electrofluorescence, yellow-green electrophosphorescence, and two-color-based white OLEDs. Journal of Materials Chemistry. 2010;20(45):10113-10119
  3. 3. Vijayan N, Babu RR, Gopalakrishnan R, Ramasamy P, Harrison WTA. Growth and characterization of benzimidazole single crystals: A nonlinear optical material. Journal of Crystal Growth. 2004;262(1-4):490-498
  4. 4. Manoharan S, Anandan S. Cyanovinyl substituted benzimidazole based (D-π-A) organic dyes for fabrication of dye sensitized solar cells. Dyes and Pigments. 2014;105:223-231
  5. 5. Saltan GM, Dincalp H, Kiran M, Zafer C, Erbas SC. Novel organic dyes based on phenyl-substituted benzimidazole for dye sensitized solar cells. Materials Chemistry and Physics. 2015;163:387-393
  6. 6. Hranjec M, Horak E, Babic D, Plavljanin S, Srdovic Z, Steinberg IM, et al. Fluorescent benzimidazo[1,2-a]quinolines: Synthesis, spectroscopic and computational studies of protonation equilibria and metal ion sensitivity. New Journal of Chemistry. 2017;41(1):358-371
  7. 7. Perin N, Nhili R, Ester K, Laine W, Karminski-Zamola G, Kralj M, et al. Synthesis, antiproliferative activity and DNA binding properties of novel 5-Aminobenzimidazo [1,2-a] quinoline-6-carbonitriles. European Journal of Medicinal Chemistry. 2014;80:218-227
  8. 8. Perin N, Uzelac L, Piantanida I, Karminski-Zamola G, Kralj M, Hranjec M. Novel biologically active nitro and amino substituted benzimidazo [1,2-a] quinolines. Bioorganic and Medicinal Chemistry. 2011;19(21):6329-6339
  9. 9. Kulhanek J, Bures F, Pytela O, Mikysek T, Ludvik J. Imidazole as a donor/acceptor unit in charge-transfer chromophores with extended π-linkers. Chemistry-An Asian Journal. 2011;6(6):1604-1612
  10. 10. Molina P, Tarraga A, Oton F. Imidazole derivatives: A comprehensive survey of their recognition properties. Organic and Biomolecular Chemistry. 2012;10(9):1711-1724
  11. 11. Wolfbeis OS. Materials for fluorescence-based optical chemical sensors. Journal of Materials Chemistry. 2005;15(27-28):2657-2669
  12. 12. Basabe-Desmonts L, Reinhoudt DN, Crego-Calama M. Design of fluorescent materials for chemical sensing. Chemical Society Reviews. 2007;36(6):993-1017
  13. 13. Horak E, Kassal P, Murković Steinberg I. Benzimidazole as a structural unit in fluorescent chemical sensors: The hidden properties of a multifunctional heterocyclic scaffold. Supramolecular Chemistry. 2018;30:838-857
  14. 14. Mohr GJ. Polymers for optical sensors. In: Optical Chemical Sensors. Vol. 2006. Dordrecht: Springer Netherlands; 2006. pp. 297-321
  15. 15. Mistlberger G, Crespo GA, Bakker E. Ionophore-based optical sensors. In: Cooks RG, Pemberton JE, editors. Annual Review of Analytical Chemistry, Vol 7. Annual review of analytical chemistry. 2014. pp. 483-512
  16. 16. Tomar PK, Chandra S, Singh I, Kumar A, Malik A, Singh A. Development of a new copper(II) ion-selective PVC membrane electrode based on tris(2-benzimidazolylmethyl)amine. Journal of the Indian Chemical Society. 2011;88(11):1739-1744
  17. 17. Yan ZN, Zhang SY, Wang HX, Kang YX. Preparation and analytical application of new Cr3+-selective membrane electrodes based on acylhydrazone-containing benzimidazole derivatives. Journal of the Iranian Chemical Society. 2016;13(3):411-420
  18. 18. Firooz AR, Ensafi AA, Karimi K, Khalifeh R. Specific sensing of mercury(II) ions by an optical sensor based on a recently synthesized ionophore. Sensors and Actuators B: Chemical. 2013;185:84-90
  19. 19. Firooz AR, Ensafi AA, Kazemifard N, Sharghi H. A highly sensitive and selective bulk optode based on benzimidazol derivative as an ionophore and ETH5294 for the determination of ultra trace amount of silver ions. Talanta. 2012;101:171-176
  20. 20. Horak E, Vianello R, Hranjec M, Krištafor S, Zamola GK, Steinberg IM. Benzimidazole acrylonitriles as multifunctional push-pull chromophores: Spectral characterisation, protonation equilibria and nanoaggregation in aqueous solutions. Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy. 2017;178:225-233
  21. 21. Horak E, Kassal P, Hranjec M, Steinberg IM. Benzimidazole functionalised Schiff bases: Novel pH sensitive fluorescence turn-on chromoionophores for ion-selective optodes. Sensors and Actuators B: Chemical. 2018;258:415-423
  22. 22. Fernandez-Alonso S, Corrales T, Pablos JL, Catalina F. A switchable fluorescence solid sensor for Hg2+ detection in aqueous media based on a photocrosslinked membrane functionalized with (benzimidazolyl)methyl-piperazine derivative of 1,8-naphthalimide. Sensors and Actuators B-Chemical. 2018;270:256-262
  23. 23. Anantha-Iyengar G, Shanmugasundaram K, Nallal M, Lee K-P, Whitcombe MJ, Lakshmi D, et al. Functionalized conjugated polymers for sensing and molecular imprinting applications. Progress in Polymer Science. 2019;88:1-129
  24. 24. Alvarez A, Costa-Fernández JM, Pereiro R, Sanz-Medel A, Salinas-Castillo A. Fluorescent conjugated polymers for chemical and biochemical sensing. TrAC Trends in Analytical Chemistry. 2011;30(9):1513-1525
  25. 25. Altarawneh S, Nahar L, Arachchige IU, El-Ballouli AO, Hallal KM, Kaafarani BR, et al. Highly porous and photoluminescent pyrene-quinoxaline-derived benzimidazole-linked polymers. Journal of Materials Chemistry A. 2015;3(6):3006-3010
  26. 26. Choi HW, Kim YS, Yang NC, Suh DH. Synthesis of a new conjugated polymer based on benzimidazole and its sensory properties using the fluorescence-quenching effect. Journal of Applied Polymer Science. 2004;91(2):900-904
  27. 27. Saikia G, Iyer PK. A remarkable superquenching and superdequenching sensor for the selective and noninvasive detection of inorganic phosphates in saliva. Macromolecules. 2011;44(10):3753-3758
  28. 28. Wu CS, Liu CT, Chen Y. Multifunctional copolyfluorene containing pendant benzimidazolyl groups: Applications in chemical sensors and electroluminescent devices. Polymer Chemistry. 2012;3(12):3308-3317
  29. 29. Han B, Zhou NC, Zhang W, Cheng ZP, Zhu J, Zhu XL. Fluorescence emission of amphiphilic copolymers bearing benzimidazole groups: Stimuli-responsive behaviors in aqueous solution. Journal of Polymer Science Part A: Polymer Chemistry. 2013;51(20):4459-4466
  30. 30. Shen LJ, Zhao P, Zhu WH. A ratiometric hydrophilic fluorescent copolymer sensor based on benzimidazole chromophore for microbioreactors. Dyes and Pigments. 2011;89(3):236-240
  31. 31. Li JX, Liu D, Hao ZC, Cui GH. An unusual (3,4,5)-connected 3D cadmium metal-organic framework as a luminescent sensor for detection of Cr2O72− in water. Inorganic Chemistry Communications. 2018;97:79-82
  32. 32. Yu Y, Zhang XM, Ma JP, Liu QK, Wang P, Dong YB. Cu(I)-MOF: Naked-eye colorimetric sensor for humidity and formaldehyde in single-crystal-to-single-crystal fashion. Chemical Communications. 2014;50(12):1444-1446
  33. 33. Zhou L, Zhao K, Hu YJ, Feng XC, Shi PD, Zheng HG. A bifunctional photoluminescent metal-organic framework for detection of Fe3+ ion and nitroaromatics. Inorganic Chemistry Communications. 2018;89:68-72
  34. 34. Dong Y, Zhang H, Lei F, Liang M, Qian X, Shen P, et al. Benzimidazole-functionalized Zr-UiO-66 nanocrystals for luminescent sensing of Fe3+ in water. Journal of Solid State Chemistry. 2017;245:160-163
  35. 35. Li S-L, Lan Y-Q , Ma J-C, Ma J-F, Su Z-M. Metal−organic frameworks based on different benzimidazole derivatives: Effect of length and substituent groups of the ligands on the structures. Crystal Growth and Design. 2010;10(3):1161-1170
  36. 36. Hao SY, Hou SX, Hao ZC, Cui GH. A new three-dimensional bis(benzimidazole)-based cadmium(II) coordination polymer. Spectrochimica Acta Part A-Molecular and Biomolecular Spectroscopy. 2018;189:613-620
  37. 37. Tripathi S, Bardhan D, Chand DK. Multistimuli-responsive hydrolytically stable “smart” mercury(II) coordination polymer. Inorganic Chemistry. 2018;57(18):11369-11381
  38. 38. Yang YS, Wang KZ, Yan DP. Ultralong persistent room temperature phosphorescence of metal coordination polymers exhibiting reversible pH-responsive emission. Acs Applied Materials and Interfaces. 2016;8(24):15489-15496
  39. 39. Zhao XX, Liu D, Li YH, Cui GH. Bifunctional silver(I) coordination polymer exhibiting selective adsorptive of Congo red and luminescent sensing for ferric ion. Polyhedron. 2018;156:80-88
  40. 40. Wei XJ, Li YH, Qin ZB, Cui GH. Two zinc(II) coordination polymers for selective luminescence sensing of iron(III) ions and photocatalytic degradation of methylene blue. Journal of Molecular Structure. 2019;1175:253-260
  41. 41. Hao JM, Yu BY, Van Hecke K, Cui GH. A series of d(10) metal coordination polymers based on a flexible bis(2-methylbenzimidazole) ligand and different carboxylates: Synthesis, structures, photoluminescence and catalytic properties. CrystEngComm. 2015;17(11):2279-2293
  42. 42. Wang XF, Du CC, Zhou SB, Wang DZ. Six complexes based on bis(imidazole/benzimidazole-1-yl)pyridazine ligands: Syntheses, structures and properties. Journal of Molecular Structure. 2017;1128:103-110
  43. 43. Jeronimo PCA, Araujo AN, Montenegro MCBSM. Optical sensors and biosensors based on sol-gel films. Talanta. 2007;72(1):13-27
  44. 44. Hoffmann HS, Stefani V, Benvenutti EV, Costa TMH, Gallas MR. Fluorescent silica hybrid materials containing benzimidazole dyes obtained by sol-gel method and high pressure processing. Materials Chemistry and Physics. 2011;126(1-2):97-101
  45. 45. Babu SS, Praveen VK, Ajayaghosh A. Functional π-gelators and their applications. Chemical Reviews. 2014;114(4):1973-2129
  46. 46. Ma XX, Xie JS, Tang N, Wu JC. AIE-caused luminescence of a thermally-responsive supramolecular organogel. New Journal of Chemistry. 2016;40(8):6584-6587
  47. 47. Yu H, Kawanishi H, Koshima H. Preparation and photophysical properties of benzimidazole-based gels. Journal of Photochemistry and Photobiology A: Chemistry. 2006;178(1):62-69
  48. 48. Shen X, Jiao T, Zhang Q , Guo H, Lv Y, Zhou J, et al. Nanostructures and self-assembly of organogels via benzimidazole/benzothiazole imide derivatives with different alkyl substituent chains. Journal of Nanomaterials. 2013;2013:8
  49. 49. Xue P, Lu R, Jia J, Takafuji M, Ihara H. A smart gelator as a chemosensor: Application to integrated logic gates in solution, gel, and film. Chemistry – A European Journal. 2012;18(12):3549-3558
  50. 50. Mondal S, Ghosh K. Anthraquinone derived cholesterol linked imidazole gelator in visual sensing of picric acid. Chemistry Select. 2017;2(17):4800-4806
  51. 51. Ghosh K, Panja S, Bhattacharya S. Visual sensing of Ag+ ions through gelation of cholesterol-appended benzimidazole and associated ion conducting behaviour. Chemistry Select. 2017;2(3):959-966
  52. 52. Yao H, Wang J, Song S-S, Fan Y-Q , Guan X-W, Zhou Q , et al. A novel supramolecular AIE gel acts as a multi-analyte sensor array. New Journal of Chemistry. 2018;42(22):18059-18065
  53. 53. Yao H, Wu HP, Chang J, Lin Q , Wei TB, Zhang YM. A carboxylic acid functionalized benzimidazole-based supramolecular gel with multi-stimuli responsive properties. New Journal of Chemistry. 2016;40(6):4940-4944
  54. 54. Hong Y, Lam JWY, Tang BZ. Aggregation-induced emission. Chemical Society Reviews. 2011;40(11):5361-5388
  55. 55. Cao YL, Yang MD, Wang Y, Zhou HP, Zheng J, Zhang XZ, et al. Aggregation-induced and crystallization-enhanced emissions with time-dependence of a new Schiff-base family based on benzimidazole. Journal of Materials Chemistry C. 2014;2(19):3686-3694
  56. 56. Gogoi A, Mukherjee S, Ramesh A, Das G. Aggregation-induced emission active metal-free chemosensing platform for highly selective turn-on sensing and bioimaging of pyrophosphate anion. Analytical Chemistry. 2015;87(13):6974-6979
  57. 57. Malakar A, Kumar M, Reddy A, Biswal HT, Mandal BB, Krishnamoorthy G. Aggregation induced enhanced emission of 2-(2 ’- hydroxyphenyl) benzimidazole. Photochemical and Photobiological Sciences. 2016;15(7):937-948
  58. 58. Wu Z, Sun JB, Zhang ZQ , Gong P, Xue PC, Lu R. Organogelation of cyanovinylcarbazole with terminal benzimidazole: AIE and response for gaseous acid. RSC Advances. 2016;6(99):97293-97301
  59. 59. Horak E, Hranjec M, Vianello R, Steinberg IM. Reversible pH switchable aggregation-induced emission of self-assembled benzimidazole-based acrylonitrile dye in aqueous solution. Dyes and Pigments. 2017;142:108-115
  60. 60. Singh A, Raj P, Singh N. Benzimidazolium-based self-assembled fluorescent aggregates for sensing and catalytic degradation of diethylchlorophosphate. Acs Applied Materials and Interfaces. 2016;8(42):28641-28651
  61. 61. Zhan Y, Wei Q , Zhao J, Zhang X. Reversible mechanofluorochromism and acidochromism using a cyanostyrylbenzimidazole derivative with aggregation-induced emission. RSC Advances. 2017;7(77):48777-48784
  62. 62. Horak E, Robić M, Šimanović A, Mandić V, Vianello R, Hranjec M, et al. Tuneable solid-state emitters based on benzimidazole derivatives: Aggregation induced red emission and mechanochromism of D-π-a fluorophores. Dyes and Pigments. 2019;162:688-696
  63. 63. Benelhadj K, Massue J, Retailleau P, Ulrich G, Ziessel R. 2-(2 ’-Hydroxyphenyl)benzimidazole and 9,10-Phenanthroimidazole chelates and borate complexes: Solution- and solid-state emitters. Organic Letters. 2013;15(12):2918-2921
  64. 64. Chaudhuri T, Mondal A, Mukhopadhyay C. Benzimidazole: A solid state colorimetric chemosensor for fluoride and acetate. Journal of Molecular Liquids. 2018;251:35-39
  65. 65. Maeda C, Todaka T, Ueda T, Ema T. Color-Tunable solid-state fluorescence emission from Carbazole-based BODIPYs. Chemistry-A European Journal. 2016;22(22):7508-7513
  66. 66. Borisov SM, Klimant I. Optical nanosensors–Smart tools in bioanalytics. The Analyst. 2008;133(10):1302-1307
  67. 67. Wolfbeis OS. An overview of nanoparticles commonly used in fluorescent bioimaging. Chemical Society Reviews. 2015;44(14):4743-4768
  68. 68. Montalti M, Rampazzo E, Zaccheroni N, Prodi L. Luminescent chemosensors based on silica nanoparticles for the detection of ionic species. New Journal of Chemistry. 2013;37(1):28-34
  69. 69. Song X, Li F, Ma J, Jia N, Xu J, Shen H. Synthesis of fluorescent silica nanoparticles and their applications as fluorescence probes. Journal of Fluorescence. 2011;21(3):1205-1212
  70. 70. Borisov SM, Mayr T, Mistlberger G, Waich K, Koren K, Chojnacki P, et al. Precipitation as a simple and versatile method for preparation of optical nanochemosensors. Talanta. 2009;79(5):1322-1330
  71. 71. Badiei A, Razavi BV, Goldooz H, Ziarani GM, Faridbod F, Ganjali MR. A novel fluorescent chemosensor assembled with 2,6-Bis(2-Benzimidazolyl)pyridine-functionalized Nanoporous silica-type SBA-15 for recognition of Hg2+ ion in aqueous media. International Journal of Environmental Research. 2018;12(1):109-115
  72. 72. Kaur N, Raj P, Kaur N, Kim DY, Singh N. Supramolecular hybrid of ZnO nanoparticles with benzimidazole based organic ligand for the recognition of Zn2+ ions in semi-aqueous media. Journal of Photochemistry and Photobiology A: Chemistry. 2017;347:41-48
  73. 73. Wang XX, Zeng FY, Ma ZY, Jiang YL, Han QR, Wang BX. Self-assembly of benzimidazole-ended nano hyperbranched polyester and its host-guest response. Materials Letters. 2016;173:191-194
  74. 74. Boonsri M, Vongnam K, Namuangruk S, Sukwattanasinitt M, Rashatasakhon P. Pyrenyl benzimidazole-isoquinolinones: Aggregation-induced emission enhancement property and application as TNT fluorescent sensor. Sensors and Actuators B: Chemical. 2017;248:665-672
  75. 75. Aich K, Das S, Goswami S, Quah CK, Sarkar D, Mondal TK, et al. Carbazole-benzimidazole based dyes for acid responsive ratiometric emissive switches. New Journal of Chemistry. 2016;40(8):6907-6915
  76. 76. Kumar G, Gupta N, Paul K, Luxami V. Acrylonitrile embedded benzimidazole-anthraquinone based chromofluorescent sensor for ratiometric detection of CN ions in bovine serum albumin. Sensors and Actuators B-Chemical. 2018;267:549-558
  77. 77. Dhaka G, Kaur N, Singh J. Spectral studies on benzimidazole-based “bare-eye” probe for the detection of Ni2+: Application as a solid state sensor. Inorganica Chimica Acta. 2017;464:18-22

Written By

Ema Horak, Robert Vianello and Ivana Murković Steinberg

Submitted: December 3rd, 2018 Reviewed: March 5th, 2019 Published: April 3rd, 2019