FTIR analysis data showing various functional groups present in dextran sulfate (DS) and AgNP‐DS complex.
The intention of this chapter is to contribute in clarification of nanoparticle synthesis and biocomplexes based on exopolysaccharide, green synthetic method development, their physico‐chemical characterization by modern spectroscopy, as well as testing of their antimicrobial activity. Silver nanoparticles of polysaccharide type have scientific interest, but practical importance too, because of their application in pharmaceutical and cosmetic product development due to proven antimicrobial and antioxidant activities. On the other hand, the biocomplexes based on exopolysaccharides are important in treatment of biometal deficiency in human and veterinary medicine, as well as in metal ion transporting in organism. Despite a number of studies of this kind of complexes, the investigations of effect of their structure to pharmaco‐biological activity are still interesting. It is important that question of interaction between reducing and stabilizing agents with metal ions is still opened. In this respect, the presented chapter offers further progress in the examination of silver nanoparticles and cobalt biocomplex synthesis with dextran oligosaccharides and its derivatives (such as dextran sulfate and carboxymethyl dextran). The complex structure, spectroscopic characterization, and the spectra‐structure correlation have been analyzed by different Fourier transform infrared (FTIR) spectroscopic techniques combined with energy‐dispersive X‐ray (EDX), X‐ray diffraction (XRD), scanning electron microscopy (SEM), and surface plasmon resonance UV‐Vis methods.
- FTIR spectroscopy
Investigation of nanoparticles by different methods, especially by Fourier transform infrared (FTIR) spectroscopy, is very interesting in last years since they have a wide potential application in different industries [1–5]. Thus, silver nanoparticles (AgNP) of polysaccharide type and other natural products have scientific interest, but practical importance too, because of their application in pharmaceutical and cosmetic products development due to proven antimicrobial and antioxidant activities [6–9]. The nanoparticles are commonly synthesized by silver (or other metals) ions reduction to elementary state. But, reducing agents should also possess stabilizing properties in order to prevent aggregation . Bankura and coworkers described a simple method of AgNP synthesis at room temperature from dextran, as well as their characterization and microbiological activity . Pullulan‐mediated Ag nanoparticles, their synthesis, characterization, and microbiological activities are also reported . Soluble starch, starch‐like polysaccharides, and chitosan are used in AgNP synthesis [5–9]. AgNP chitosan/gelatin bionanocomposites have also been studied . Compounds containing carbonyl group are relatively easy complexed with different metals [10–12]. This functional group contains some polysaccharide derivatives like carboxymethyl cellulose (CMC) or carboxymethyl dextran (CMD), which are obtained by different chemical reactions of proton exchange between OH groups of glucoside moiety and carboxymethyl groups. AgNP‐CMC nanoparticles were prepared in weak alkaline solution by reaction of AgNO3 with CMC as a reducing and capping agent. It has been established that size distribution and morphology of mentioned nanoparticles are depended on Ag: CMC weight ratio, reaction time, temperature, and pH value of the reaction system. FTIR spectrophotometric analysis has shown that interactions between AgNP and polysaccharide have steric character . Studies of composite hydrazine‐CMD and CMD magnetic Fe‐based nanoparticles [14, 15] have shown that solubility of these nanoparticles depends on pH value (NaOH), not on CMD content. This fact indicates on strong interactions of carbonyl group with magnetic nanoparticles on the surface.
Hence, there are indications that carboxymethyl dextran form nanoparticles with Ag ions. CMD possess COOH group which can react with positively charged Ag ions to form complex compounds, but, it can also reduce Ag ions and stabilize the formed nanoparticles as in the case of hyaluronic acid with AgNP . Since CMD has the ability to form nanoparticles, the intention of this chapter is to contribute in clarification of AgNP synthesis, physico‐chemical characterization by FTIR spectroscopic, diffraction and chromatographic methods, as well as testing of their antimicrobial activity. On the other hand, the biocomplexes based on exopolysaccharides are important in treatment of biometals deficiency in human and veterinary medicine [1, 17]. Polysaccharides, oligosaccharides and their derivatives, as well as simple sugars, may be used as ligands for the synthesis of biocomplexes with different metal ions (Cu, Fe, and Zn). These biocomplexes have an important role in metal ions transporting in organism . Despite a number of studies of this kind of complexes, the investigations of effect of their structure to pharmaco‐biological activity are still interesting . In this respect, the presented chapter offers further progress in the investigation of cobalt complex synthesis with dextran oligosaccharide, spectroscopic characterization, and the spectra‐structure correlation by various FTIR techniques.
2. Green nanoparticles of silver
Recent investigations of nanoparticles synthesis are mostly directed to green synthetic methods development. These methods include nontoxic reagents, synthesis procedures without problematic side products, and especially usage of biodegradable materials. Thus, chemical reduction in silver ions is the most frequently used besides photochemical or electrochemical methods . In order to reduce and stabilize the Ag nanoparticles, the polysaccharides (dextran, starch, pullulan, cellulose) and their derivatives (dextran sulfate-DS, carboxymethyl cellulose, carboxymethyl dextran, chitosan, hyaluronic acid, heparin), and biocomposites AgNP chitosan/gelatin, are developed and improved [2–6, 13, 14, 16, 20–25]. Characterization of these particles has been carried out by UV‐Vis, FTIR spectroscopy, X‐ray diffraction (XRD), and energy‐dispersive X‐ray (EDX) methods. Electronic microscopy techniques [scanning electron microscopy (SEM) and TEM] are used for particle size determination and distribution, as well as shape defining. It is interesting that question of interaction nature between reducing and stabilizing agents with AgNP is still opened. Some authors  consider that steric physical interactions are relevant, while others [2, 16] give an explanation via coordination complex of Ag ions with reducing and stabilizing agents which contain suitable functional groups (COOH, NH2, OH, OSO3H), as in the case of Cu(II) ions complexes with carboxymethyl dextran or dextran sulfate (Figure 1).
Having in mind these facts, it can be assumed that dextran sulfate, which contains one or more sulfo groups in its structure, can be used as reducing and stabilizing agent for the AgNP synthesis. Also, it may be assumed that dextran sulfate forms complexes similar to CMD about what there are no literature data. Therefore, investigations in this chapter are related to the AgNP‐DS and AgNP‐CMD synthesis, their characterization by different methods and antimicrobial activity determination.
2.1. Synthesis procedure
The synthesis of AgNP‐DS has been performed in a reactor at temperature of 100°C, during 240 min, at constant pH of 7.5 and continuously stirring. Dextran sulfate has been used as a ligand in the synthesis. The synthesis is performed by DS solution (100 cm3, 0.002 M) adding in 100 cm3 of AgNO3 solution (0.001 M). The complex formation has been monitored via changing of reaction solution color, from white to yellow. The AgNP‐DS complex was precipitated with 96% ethanol after cooling down the reaction mixture to the room temperature. The obtained product has been dried at105°C under vacuum during 180 min. On the other hand, the carboxymethyl dextran has been used in the case of the AgNP‐CMD complex synthesis. The synthesis has been performed by 100 cm3 of AgNO3 (0.001 M) solution adding in 200 cm3 of CMD ligand solution (0.002 M) at constant pH of 7.0 (adjusted by NaOH). The synthesis is performed to the defined M:L ratio (from 1:1 to 1:2) by changing of reagents volume. The complexation has been performed at 100°C and continuously stirring during 120 min. A successful outcome of the AgNP‐CMD complex synthesis has been identified by changing of reaction solution color, from white to yellow. The reaction mixture has kept under reflux 24 h more, after that it has cooled to room temperature, and the complex AgNP‐CMD has precipitated by 96% ethanol. Final product has been dried at 105°C under vacuum during 180 min. The prepared AgNP‐DS and AgNP‐CMD complexes were characterized by different methods (FTIR, UV‐Vis, SEM, XRD, EDX) and by antimicrobial activity.
2.2. FTIR study
The FTIR spectra were recorded by BOMEM MB‐100 (Hartmann & Braun, Canada) FTIR spectroscope and by KBr technique, at room temperature with 2 cm-1 resolution. Spectra‐structure correlation has been performed on empirical manner [2, 22], by comparing the spectra of ligands (DS and CMD) with the spectra of their complexes (AgNP‐DS and AgNP‐CMD). The appropriate FTIR spectra are shown in Figures 2 and 3.
The results of the complex AgNP‐DS spectral analysis are shown in Table 1. They show the position and assignations of bands that come from vibrations of all types of sulfo groups in DS and AgPN‐DS, as well as bands of deformation CH vibrations outside of the plane of glucopyranose unit which are characteristic for its conformation determining. As it can be seen in Table 1, there is a difference in the position of the νas(S–O) band which is shifted ~22 cm-1 toward lower frequencies in the AgPN‐DS spectrum (Figure 2), as well as the band from νas(O–S–O) which is shifted ~8 cm-1 toward higher frequencies. This difference in the bands position indicates the formation of coordination complexes between Ag ions and DS, where there is a change in conformation of sulfo groups from Eq to Ax position. The appearance of the spectrum in the area of C–CH out‐of‐plane deformational vibrations surface coupled with C–C–O, O–C–O and C–O–C vibrations depends on glucopyranose unit conformation [25–27]. When it is 4C1 conformation, the bands at ~915 cm-1 (weak), 850 cm-1 (shoulder), and 752 cm-1 are expected in the spectrum. The results from Table 1 show that starting DS retains the same conformation of glucopyranose unit during complex with Ag ions formation. There is a sharp intensive band at 1384 cm-1 in the FTIR spectrum of AgNP‐DS (Figure 2) observed by other authors who have investigated similar complexes and given the explanation of its origin [4, 5, 13, 22]. So, in the case of AgNP‐CMD complex (Figure 3c), some authors consider that this band is a result of νs(O–N–O) at O=NO2 − radicals which are formed from AgNO3 agents participating in the formation of nanoparticles through the surface interactions .
|Assignation||DS (cm-1)||AgNP‐DS (cm-1)||Δν (cm-1)|
|4C1 conformation of the α‐d‐glucopyranose ring||915||915||–|
The infrared spectra of AgNP‐CMD products and starting CMD agent are compared with literature data and dextran spectrum because of the major bands assignment (Figure 3). In the CMD spectrum, vibrations of carboxymethyl groups: ν(C–O) around 1740 cm-1; deformation vibration δ(C–OH) which appears around 1250 cm-1; ν(C–O) vibration around 1150 cm-1; and deformation δ(C–O) vibration around 680 cm-1 are expected to oppose starting dextran for CMD synthesis. Stretching ν(C–O) vibration has been found in similar carboxymethyl polysaccharides; after carboxymethylation of the k‐carrageenan, ν(C–O) has found at 1737 cm-1 , for carboxymethylated glucan at 1736 cm-1 , as well as at 1750 cm-1 in the spectrum of CMD . As it can be seen from Figure 3b, the CMD spectra possess bands at 1740, 1244, 1139, and 682 cm-1 (which are marked by arrows) from CO carboxymethyl vibration of all types. The aforementioned bands are not in the range of dextran (Figure 3a) as it is expected. Changes in the position of the above‐mentioned bands can be a good indicator of bonds type that is eventually formed by interaction with Ag+ ions . Also, the changes in the area of deformation vibration of C–OH are expected. In the case of AgNP‐CMD coordination complexes formation, the frequency ν(C–O) band should be lower, or, if both O atoms of COOH groups participate in the coordination, the frequency of ν(C–O) vibration should be higher because of electron delocalization, as well as the absence of δ (C–OH) bands.
Speaking about carboxylate anion, delocalization of electrons causes the order of two CO bonds to be the same, so two bands (at 1600 and 1400 cm-1) are expected in CO stretching vibration region, which are ascribed to asymmetric and symmetric C–O vibration, as it is indicated in the literature [13, 16, 28]. The similar situation is in AgNP‐CMD complex (Figure 3c) in the CO groups vibration area. In fact, in this area of the spectrum, there are two intensive bands (at 1603 and 1420 cm-1) which, according to its position and intensity should be attributed, νas(C–O) and νs(C–O) vibration, indicating coordination of Ag+ ions with a COOH group. In support of this is the absence of ν(C–O) and δ(C–OH) vibration bands. The appearance of spectrum in the area of 1000–700 cm-1, in all three tested compounds (Figure 3), is very similar and according to the literature data [30, 31] suggests 4C1 conformation of the glucopyranose unit.
2.3. UV‐Vis study
Absorption spectra of starting ligand compounds (DSi CMD) as well as of final complexes (AgNP‐DS and AgNP‐CMD) are obtained by UV‐Vis spectrophotometer (Varian Cary‐100 Conc.). Spectrophotometric analysis was carried out in the range of 200–800 nm using original Cary UV‐Conc. (Varian) software. The obtained UV‐Vis spectra are presented in Figures 4 and 5.
Change in color from yellowish to brown, as well as careful interpretation of UV‐Vis spectra, is used for estimating of AgNP synthesis [2–10]. A strong absorption band, called SPR band (surface plasmon resonance), is expected in 370-450 nm region in the UV‐Vis spectrum of AgNP . Its exact position depends on numerous factors (the most on AgNP size), while intensity depends on their concentration [4, 21, 33]. Changes in this band position are used as a criterion of the AgNP stability, that is, aggregation of the nanoparticles during the time. As it can be seen from Figure 4, the existence of SPR band at 410 nm indicates the AgNP formation. However, its position is changed during synthesis with time, but after 2 h remains constant at 420 nm. The estimated particle size of AgNP‐DS based on the UV data  is approximately 40 nm. A change in color from yellowish to brown during the synthesis has been observed in the case of AgNP‐CMD formation. SPR band for this complex (Figure 5), synthesized at different molar ratio, is located at 420 nm, which is not present in the starting CMD. It is characteristic that intensity of this band is proportional to the amount of AgPN‐CMD particles; it increases with increasing amounts of CMD, or during staying of the reaction mixture for 3 months (Figure 5C), which is similar to other studies . Unchanged position of SPR band speaks in favor of good aggregation stability of synthesized particles. UV area below 300 nm was not investigated in the literature. However, in the UV spectra of tested compounds (Figure 5), there is an intense band of the formed complex at 215 nm (π→π* transition of the carboxyl group ) indicating red shift effect compared to CMD. This phenomenon is an indicator of Ag ions interaction with CMD and AgNP‐CMD complex formation.
2.4. XRD study
Crystal structure of AgNP‐DS and AgNP‐CMD nanoparticles was determined and confirmed by X‐ray diffraction (XRD) technique. The samples were prepared by press and pull method in top‐loading specimen plate . The diffractogram was measured in Bragg‐Brentano θ: 2θ geometry by a conventional powder diffractometer, Seifert V‐14, using Cu Kα radiation (λCu Kα1 = 1.5406 Å, Ni filter, generator settings: 30 kV, 30 mA). As an external standard for peak position calibration and instrumental peak broadening determination, LaB6 was used. XRD data were collected over the 2θrange of 5–90°with a step size of 0.02°, and an exposition time of 2 s per step. The obtained diffractograms are shown in Figures 6 and 7.
From the presented X‐ray diffraction patterns of AgNP‐DS (Figure 6) can be noticed the XRD peaks at 38.24, 44.32, 64.58, 77.59,and 81.79°. Based on literature data [4, 6], the characteristic XRD peaks could be determined as next crystallographic planes: 111, 200, 220, 311, and 222. These planes are specific for the face‐centered cubic silver crystals. This statement, along with the specified values, indicates the presence of silver nanoparticles in the synthesized AgNP‐DS complex. Similar to the previous study, the crystal structure of Ag nanoparticles was determined with complex AgNP‐CMD. Based on X‐ray diffraction patterns (Figure 7) and the presence of XRD peaks at 38.02, 44.50, and 64.51°, a particular crystallographic planes are as follows: 111, 200, and 220, which are specific for the cubic silver crystals. According to literature [4, 6], the XRD peak at 29.01° is characteristic of the CMD ligand.
The calculation of average AgNP size has been done from the width of reflection in the X‐ray diffraction pattern according to the Scherrer's equation (1):
2.5. SEM and EDX study
The size and shape of AgNP‐DS and AgNP‐CMD complexes were further characterized by scanning electron microscopy (SEM) on JEOL JSM 5300 scanning electron microscope. Scanning micrographs were transformed into a PC format in order to further analyze the particles morphology. The samples for SEM analysis have been prepared by thin layer of the complex suspension overnight air drying at room temperature. Dried samples have been coated with 10‐nm‐thick film of gold in JPC JEOL‐1100 apparatus. Electron beam of 30 keV has been used. The SEM micrographs of AgNP‐DS (Figure 8A) showed both individual particles, but a number of aggregates, too. Size of 10–60 nm is predominant for individual spherical particles. Images have also indicated that obtained nanoparticles are stable, and they are not in a mutual contact. This can be ascribed to stabilization of the nanoparticles by DS as a capping agent. Aggregates of nanoparticles with poorly defined morphology and irregular structure have also been found (Figure 8A).
Energy‐dispersive X‐ray (EDX) spectral analysis has been performed by LINK Analytical 2000 QX microprobe assembled on a JEOL JSM 5300 scanning electron microscope. Samples prepared for SEM analyses have been used for EDX spectra measuring. EDX spectroscopy can be used for qualitative as well as quantitative assessment of silver used for the AgNP production . EDX spectrum of AgNP‐DS is shown in Figure 8B. Strong signal comes from elemental silver, while weaker signals come from S, O, and Na (from Na salt of DS), confirming that AgNP are formed as a part of AgNP‐DS. This is consistent with an optical absorption peak appearance at approximately 3 eV (410 nm), which originates from SPR, and it is characteristic for metallic silver nanocrystals .
Similar to the previous complex, the SEM micrographs of AgNP‐CMD (Figure 9A) show single particles, but a number of aggregates as well. Particle size of 10–60 nm is dominant for individual spherical particles. SEM images showed that obtained nanoparticles are stable and not in direct contact with each other. This can be explained as stabilization effect of CMD, as a capping agent, on produced nanoparticles. But, aggregated nanoparticles with larger irregular structure and no well‐defined morphology were also found (Figure 9B).
2.6. Antimicrobial study
Agar disk diffusion method has been used for measuring of antibacterial and antifungal activity of AgNP stabilized by DS. One fungal strain (
|0.25 mg cm-3||0.5 mg cm-3||1.0 mg cm-3|
The investigated AgNP‐DS solution has shown antibacterial activity against
|0.25 mg cm-3||0.5 mg cm-3||1.0 mg cm-3|
In order to compare antimicrobial activity of similar complexes, the results of AgNP‐CMD antimicrobial activity (radial diameter of inhibition zones) are presented in Table 3. The AgNP‐CMD solution exhibited antibacterial activity against bacteria
3. Cobalt(II)‐dextran biocomplexes
A lot of investigations in the field of coordination chemistry are based on synthesis and characterizations of different biocomplexes present in the biological systems. Synthetic ligands, which can serve as model molecules for complex biomolecular structures, are also investigated . Bioligands or synthetic ligands are mostly natural macromolecular compounds. These products of special importance mostly represent complexes of different metals (Fe, Co, Cu, Zn) with ligands of polysaccharide type (such as pullulan, inulin, dextran) [43–45]. However, the native polysaccharide possessing antigen characteristics wherefore is not of pharmaceutical importance . Depolymerization of raw polysaccharides, trying to get products with adequate molar masses distribution for commercial purposes, has been done. Dextran, is a well‐known, extracellular, water‐soluble neutral polysaccharide with α‐(1–6)‐linked d‐glucopyranose unit chain, with a wide range of applications. Dextran gained from
3.1. Complex synthesis
The cobalt complexes with reduced low‐molar dextran as ligand (Co(II)‐RLMD) were synthesized in water solutions, at different pH values (7.5-13.5) and different temperatures (298–373 K), using CoCl2 × 6H2O and RLMD (5000 g/mol). The details of synthesis have been described [54, 55]. The complexes were isolated in the solid state. For further structural examination, the samples of Co(II)–RLMD were deuterated (D2O, Merck) for 2 h, at room temperature, in vacuum.
3.2. FTIR study
KBr pastille method has been used for sample preparation. The FTIR spectra have been recorded at room temperature, as an average value of 40 scans (resolution of 2 cm-1) on a Bomem MB‐100 FTIR spectrometer (Hartmann & Braun, Canada) coupled with a DTGS/KBr detector. Spectra‐structural correlation of dextran by FTIR spectroscopy has been the subject of attention of many researchers [30, 31, 56–58]. It was shown that by studying the individual spectral areas, the information on linearity [content of α‐(1–6) bond], crystallinity, conformation, conformational transitions, and changes in the structure of differently treated dextrans can be obtained. The FTIR spectrum of reduced low‐molar dextran is shown in Figure 11a. Bands at 765 and 916 cm-1 are indicating the presence of the α‐(1–6) glycosidic bonds, and the estimated content of these bonds is greater than 96% that indicates a high linearity of polysaccharide. The presence of these bands as those at the 845 cm-1 indicates a C1 conformation of glucopyranose units (eq‐ax‐ax‐ax‐ax arrangement of adjacent C–H groups). There is an intense broad band whose centroid is at about 3400 cm-1, in the area of stretching OH vibrations. Summary intensity of this band comes from the ν(O-H) vibrations of hydroxyl groups involved in the formation of several by the strength of hydrogen bonds, but also from the H2O molecule whose presence is confirmed by the band at 1640 cm-1, which is result of δ(HOH) vibrations .
The FTIR spectra of synthesized Co(II)‐RLMD complex, which were obtained under various reaction conditions, are presented in Figure 10. The FTIR spectra of RLMD and its Co(II)‐RLMD complex are basically similar. In the FTIR spectra of synthesized complex, there are the differences in the area of O–H vibrations. In this area, there is a large, complex band approximately 3390 cm-1 of ν(O–H), which is likely due to the stretching vibrations of polysaccharide OH groups. The characteristic IR band of δ(HOH) at about 1645 cm-1 in the spectra of synthesized complexes, as well as in the spectrum of RLMD, as noted above, indicates the presence of crystal water in the structure [54, 55]. By analyzing the low‐frequency part of the RLMD spectrum (γ(C-H) vibrations, Figure 10a), the FTIR spectra of Co(II)‐RLMD complex (Figure 10b and c), and the presence of bands at about 915 and 845 cm-1, 4C1 conformation of glucopyranose units, which indicates that the complexation with Co(II) ions does not lead to conformational changes in glucopyranose units, can be determined. In accordance with this is the change in the intensity of IR band in the area approximately 1350 cm-1 that originates from δ(C-H) and δ(O-H) vibrations. With an increase in the pH synthesis (from 7.5 to 13.5), the band intensity of ν(O-H) vibration increases, and the frequency of ν(O-H) vibration band at lower pH (7.5–8.5) stays almost unchanged and then increases with increasing pH (11–13.5). If the complexation with Co(II) ions takes place via OH groups at the C–2, C–3, or C–4 carbon atoms of dextran glucopyranose units (involved in the formation of various by the strength of hydrogen bonds in dextran), hydrogen bonds disappear by complexation, so the bands are expected at the higher frequencies. In complexes with the highest metal content (10.07% Co), which were synthesized at pH 12, a set of IR bands in this area is close to that at starting RLMD. In the complex which was synthesized at pH 13 with a minimum cobalt content of 1.89% in the IR spectrum (Figure 10c), there are intense bands at 3400 cm-1 to the binder of low‐frequency side in this region. This could indicate that the structure of this complex differs slightly from the structure of other Co(II)‐RLMD complex, which were synthesized under different reaction conditions. In the low‐frequency area (<800 cm-1) of the FTIR spectra of RLMD and Co(II)‐RLMD complex, there are some differences. In this region of the IR spectrum, in addition to the band of ν(Co-O), the bands of deformation γ(O-H) vibrations of polysaccharide as well as the deformation vibrations of glucopyranose ring are expected (Figure 10). Wide band of medium intensity in the FTIR spectra of Co(II)‐RLMD complex at about 450 cm-1 shows a fine structure.
3.3. Isotopic D2O exchange study
Isotopic substitution of hydrogen atoms by deuterium, connected with FTIR spectroscopy, has an important role in determining the structure of dextran. Isotopic exchange results indicate that dextran and its Co(II)‐RLMD complex are crystal hydrates (probably one type of water molecules) . Structural changes in the process have been detected by absorption bands in the area of 3600–3000 cm-1, caused by ν(O-H) vibrations. In the case of isotopic exchanges of O-H to O-D group, the frequency of stretching vibration is reduced to √2, and it is located in the area of 2700–2300 cm-1. Deuteration is a very sensitive method to assess the environment of OH groups, which is associated with the intensity generated by hydrogen bonds. The degree of crystallinity of the polysaccharide can be determined by FTIR spectroscopy method with deuteration. Crystallinity is a part of the regulated saccharide area in which the macromolecules are connected with parallel hydrogen bonds. In processing the sample with D2O, usually OH groups in less regulated or amorphous regions were rapidly converted into OD groups. Conversion of OH groups in the crystal areas is very slow. Thus, the degree of crystallinity has been determined by the change in intensity of asymmetrical ν(O-H) band vibrations and by the appearance of new bands of ν(O-D) vibration. The relations of band intensity at 1429 and 893 cm-1 were taken as empirical indicators of the degree of crystallinity of samples. With decrease in the crystallinity, the band at about 1430 cm-1 disappears and comes to an increase in the intensity of the band at approximately 900 cm-1, typical for the amorphousness. Even better relationship can be seen at the band at approximately 1370 and 2900 cm-1. Namely, in the spectrum of partially deuterated analogs of dextran (Figure 11) in the ν(O-D) area of the vibration of HDO molecules, there is a single band at about 2495 cm-1. Partners of these vibrations would be expected at about 3400 cm-1 in the ν(O–H) areas (taking into account the displacement factor of 1.35).
The FTIR spectra of Co(II)‐RLMD complex (a) and its deuterated analog (b), which was synthesized at pH 13, are shown in Figure 12. In the FTIR spectrum of Co(II)‐RLMD complex (Figure 12b), in the area of ν(O-D) vibrations of HDO molecules, there is a single band at about 2483 cm-1 in the corresponding complexes with crossfold on the high‐frequency side. Partners of these vibrations would be expected at about 3400 cm-1 in ν(O-H) area. Results of partial deuteration indicate that the band at about 3400 cm-1 is sensitive to isotopic substitution, in both cases (RLMD and Co(II)‐RLMD complexes). Reducing the intensity of this band by deuteration demonstrates that the ν(O-H) vibrations of water molecules are its part. This fact indicates that both compounds contain crystal water in their structure. Confirmation of this conclusion is that in the spectra of deuterated analogs of both compounds (Figures 11 and 12), an intense band near 1645 cm-1 is also highly sensitive to isotopic substitution and is to be attributed to the HOH deformation vibration of the crystal water.
As known, Seidl et al.  proposed criteria according to which, based on the study of spectra of protonated, partially and fully deuterated hydrate, it is possible to determine the number of types of H2O molecules (n) and the number of nonequivalent OH groups (m). By the spectra appearances, in the stretching OD area of HDO molecules, and the appearance of a band, whose intensity increases monotonically with increasing degree of deuteration when the frequency does not change, it can be concluded from the above criteria  that in the structure of dextran and its complexes with Co(II) ions is present one crystallographic type of water molecule (n = 1). On the basis of Berglund correlation , from equation (3), Ow…O distances are estimated at 283.1 pm for dextran and 281.8 pm for Co(II)‐RLMD complex:
Water protons are involved in the formation of relatively weak hydrogen bonds (m = 1). In bending area of HDO and D2O, in the spectrum of deuterated analogs of the complex, there are bands around 1315 and 1070 cm-1, which confirm the previously disclosed consideration of the water binding. From FTIR spectrum shown in Figure 12b, decrease in the intensity of the band around 1430 cm-1 and an increase in the band intensity at approximately 910 cm-1 can be observed, which is a characteristic for amorphous character. An even better relationship can be observed in the FTIR spectrum of Figure 12, with the band of about 1370 and 2900 cm-1. Based on the results of FTIR spectroscopy, an amorphous structure of the synthesized Co(II)‐RLMD complex can be assumed.
3.4. ATR‐FTIR microscopy study
The ATR‐FTIR spectral analysis has been performed by microspectroscopy ATR‐FTIR system (Bruker, Tensor‐27). Within this system, FTIR spectroscope is connected to a microscope (15× objective) (Bruker, Hyperion‐1000/2000) and a computer system capable of microanalysis by using a liquid‐nitrogen‐cooled (250 μm) MCT detector (GMBH, Germany). The ATR‐FTIR spectra (Kubelka‐Munk option) have been recorded in the range of 4000–400 cm-1, with 4 cm-1 resolution and 260 scans. The newly formed FTIR vibrational microspectroscopy can provide information on the sample at the molecular level, with high spatial resolution at the microscopic level. Small sample can be analyzed by both nondestructive vibrational spectroscopic techniques (Raman, IR) [62–67]. Spectra can be recorded continuously in different parts of the microsample in order to obtain appropriate databases. Figures 13 and 14 show the absorption ATR‐FTIR spectra of Co(II)‐RLMD complex, which were obtained under various reaction conditions.
The wavenumber values of characteristic IR bands in the ATR‐FTIR spectra of Co(II)‐RLMD complex are given in Table 4.
|Wavenumber (cm-1)||Band assignation||Intensity||Comment|
|3400||ν(O-H)||Very strong, complex||CH-OH glucopyranose, H2O|
|2930||νas(C-H) i νsy(C-H)||Medium||CH|
|1150, 1110, 1070, 1040, and 1010||νas(C-O), (C-O-C), νas(C-C-C) i (C-C-O)||Very strong, strong||Glucopyranose|
Absorption bands corresponding to the specific chemical components can be represented as a map. ATR‐FTIR spectra, presented in Figures 13 and 14, correspond to the different parts of the sample of Co(II)‐RLMD complex, which show a homogeneity of the samples. A new way of visualization shows the capability of visualization not only of heterogeneous region of the samples, but also at the same time provides microspectroscopic spatial information. The visualization of different concentrations of components and presentation as 3D maps is also enabled. Application of ATR‐FTIR microscopy to Co(II)‐RLMD complex, which were synthesized under different reaction conditions, is shown in Figure 15. The changes in color contours at certain parts of the image indicate the content and distribution of cobalt and polysaccharides in Co(II)‐RLMD samples. ATR‐FTIR microspectroscopic data show a high homogeneity of the samples, and the presence of Co(II) ions (the results obtained by other spectroscopic techniques) has been confirmed by the color of Co(II)‐RLMD complex.
The modern Fourier transform infrared spectroscopic techniques (linear scan, reflection, transmission, mapping, video analysis) in combination with diffraction (XRD), energy‐dispersive X‐ray (EDX), spectrophotometric (UV‐Vis), and electronic microscopy (SEM) methods are applied in the structure analysis of synthesized green nanoparticles and polysaccharide complexes, as well as for the confirmation of suggested types of complexes structure and for the testing of samples homogeneity. In this respect, silver nanoparticles were prepared with dextran sulfate or carboxymethyl dextran as a reducing and capping agent, while cobalt biocomplexes were synthesized with reduced low‐molar dextran as ligand. Comparison of FTIR spectra of initial exopolysaccharide compounds (DS, CMD, RLMD) and final products (AgNP‐DS, AgNP‐CMD, Co(II)‐RLMD complexes), in the specific region of characteristic functional group vibrations, has indicated on coordination complexes forming as a part of complex structure. FTIR spectroscopic analysis has shown that interactions between metal ions and specific polysaccharide functional groups have steric character and suggest 4C1 conformation of the glucopyranose unit. The existence of nanoparticles (in range of 10–60 nm) has been confirmed by SPR band in the UV‐Vis spectra, by SEM microscopy, and XRD methods. AgNP size was determined on the Bragg reflection at 38.24°2θ, yielding mean crystallite size of 40 ± 4 nm. It has been found that crystalline structures of silver complexes are face‐centered cubic type by XRD method. Morphological SEM analysis has been shown that formed nanoparticles are spherical and inclined to aggregation. It has been established that size distribution and morphology of mentioned nanoparticles (by SEM and FTIR microspectroscopy methods), as well as the structural form of the complexes (by FTIR, UV‐Vis, XRD), are depended on ligand properties (such as constitution, degree of amorphousness or crystallinity, molar mass, units conformation, chain linearity) and on the reaction conditions (such as metal‐ligand weight ratio, reaction time, temperature, and pH values). Also, antimicrobial and antifungal activities of synthesized AgNP have been determined. The highest inhibition zones were observed against
This study is the result of the project TR‐34012, funded by the Ministry of Education, Science and Technological Development, of the Republic of Serbia.