Open access peer-reviewed chapter

Introductory Chapter: Metal Organic Frameworks (MOFs)

By Eram Sharmin and Fahmina Zafar

Reviewed: July 4th 2016Published: October 12th 2016

DOI: 10.5772/64797

Downloaded: 3915

1. Introduction

Over the past 50 decades, porous materials, from zeolites, coordination polymers to metal organic frameworks (MOFs), have gained considerable attention. The interesting feature is their porosity that allows the diffusion of guest molecules into the bulk structure. The shape and size of pores govern the shape and size selectivity of the guests to be incorporated. MOFs as defined by Yaghi et al. are porous structures constructed from the coordinative bonding between metal ions and organic linkers or bridging ligands (Figure 1) [1]. MOFs are formed by anchoring metal‐containing units or secondary‐building units (SBUs) with organic linkers, by coordination, yielding open frameworks that show exceptional feature of permanent porosity, stable framework, enormous surface area, and pore volume. The porosity is a consequence of long organic linkers that confer large storage space and numerous adsorption sites within MOFs. They also bear the ability to systematically vary and functionalize their pore structure [2, 3]. In the history of MOFs, a benchmark was represented by the synthesis of MOF‐5 (Zn4O(bdc)3, bdc = terephthalate) and HKUST‐1 (Cu3(btc)2, btc = 1,3,5‐benzenetricarboxylate) with high porosity and low pressure gas sorption, followed by the development of chromium(III) terephthalate (MIL‐101) with high chemical stability, MOF‐74 (Zn2(dhbdc), dhbdc = 2,5‐dihydroxy‐1,4‐benzenedicarboxylate) with low pressure adsorption of CO2, and several isostructural analogs of Mg‐MOF‐74 termed as IRMOF‐74‐I to IRMOF‐74‐XI, with large pore apertures to accommodate protein, NU‐110E with acetylene‐expanded hexatopic linker, having material highest experimental Brunauer‐Emmett‐Teller (BET) surface area of any porous material reported to date (7140 m2 g-1) Some examples of MOFs and their applications are given in Table 1 [115].

Figure 1.

Structure of MOF.

ApplicationMOF Metal LigandYear Author Rf
Drug deliveryMIL‐101 [Cr3O(OH,F,H2O)3(1,4‐bdc)3 and MIL‐100Cr 1,4‐benzenedicarboxylate moieties (bdc) or H3btc: Benzene‐1,3,5‐tricarboxylate2006Patricia Horcajada et al. [4]
MOF‐5 Zn4(1,4‐bdc)3Znbdc2002Li and Eddaoudi, et al. [5, 6]
and storage
HKUST( Hong Kong University of Science and Technology)‐1 Cu2(H2O)2(CO2)4CuH3btc2006Rowsell and Yaghi [7]
and storage
IRMOF‐9 Zn4O(bpdc)3Zn4,4′‐biphenyldicarboxylate (bpdc)2006Rowsell and Yaghi [7]
and storage
MOF‐74, Zn2(C8H2O6)Zn2,5‐dihydroxybenzene‐1,4‐dicarboxylic acid2006Rowsell and Yaghi [7]
(In) MIL‐68‐NH2 or IHM‐2Inbdc‐NH2: 2‐aminoterephthalates2011Savonnet and Farrusseng [8]
metal–organic Zn(bix) spheres with encapsulated DOX [DOX/Zn(bix)],
SN‐38 [SN‐38/Zn(bix)], CPT [CPT/Zn(bix)] and DAU [DAU/Zn(bix)] Doxorubicin (DOX), SN‐38, camptothecin (CPT) and daunomycin (DAU) 
ZnBix: 1,4-bis(imidazol-1-ylmethyl)benzene2010Inhar Imaz et al. [9]
coupling–deprotection sequence
(In) MIL‐68‐NH‐ProFmoc and (In) MIL‐68‐NH‐Ala‐FmocIn *fluorenylmethyloxycarbonyl group (Fmoc), a base‐label protecting group for aminesInAmino acid such as l‐proline (Pro‐OH) and D‐alanine (Ala‐OH)2011Jerome Canivet et al. [10]
AntibacterialCu‐BTC(MOF‐199)CuH3btc2014Rodrıguez et al. [11]
Highly potent bacteriocidal activityCo‐TDMCoH8 tdm: tetrakis [(3,5‐dicarboxyphenyl)‐oxamethyl] methane2012Wenjuan Zhuang et al. [12]
Delivery of nitric oxideMIL‐100(Fe or Cr)
and MIL‐127(Fe)
Fe, Cr or Fetricarboxylate or tetracarboxylate2014Eubank et al. [13]
AntibacterialAg2(O‐IPA)(H2O)·(H3O) and Ag5(PYDC)2(OH)AgHO‐H2ipa = 5‐hydroxyisophthalic acid and H2pydc = pyridine‐3, 5‐dicarboxylic acid2014Xinyi Lu et al. [14]
Adsorption of CO2 over N2Mn3(HCOO)6 ·DMFMn3‐nitrophthalic acid (H2npta) and 4,4′‐bipyridine (4,4′‐bipy)2014Ying‐Ping Zhao et al. [15]

Table 1.

Some examples of MOFs and their applications.


2. Chemistry

MOFs consist of both inorganic and organic units. The organic units (linkers/bridging ligands) consist of carboxylates, or anions, such as phosphonate, sulfonate, and heterocyclic compounds (Figures 2 and 3). The inorganic units are the metal ions or clusters termed as SBUs. Its geometry is determined by the coordination number, coordination geometry of the metal ions, and the nature of the functional groups. A variety of SBU geometries with different number of points of extension such as octahedron (six points), trigonal prism (six points), square paddle‐wheel (four points), and triangle (three points) have been observed in MOF structures (Figure 4). In principle, a bridging ligand (ditopic, tritopic, tetratopic, or multitopic linkers) reacts with a metal ion with more than one vacant or labile site. The final framework topology of MOF is governed by both SBU connectors and organic ligand linkers. Depending upon the nature of the system used, infinite‐extended polymeric or discrete‐closed oligomeric structures can arise (Figure 4). Metal‐containing units and organic linkers can be varied resulting in a variety of MOFs, tailored for different applications [3]. MOFs with large spaces may result in the formation of interpenetrating structures. Thus, it is very important to inhibit interpenetration by carefully choosing the organic linkers. The pore size is allowed to be tuned and spatial cavity arrangement be controlled, by judicious selection of metal centers and organic ligands and also by adjusting their conditions of synthesis. The large porosity allows their applications in adsorption and separation of gaseous molecules, catalysis, microelectronics, optics, sensing applications, bioreactors, drug delivery, and others. MOFs have pore openings up to 2‐nm size, which can accommodate small molecules. However, the pore openings rarely allow the inclusion of large molecules (e.g., proteins and enzymes). Attempts have been taken to increase the pore size to mesopore regime (pore size of 2–50 nm) and to decrease the crystal size to the nanometer scale. The large pore aperture benefits surface modification with a number of functionalities, without sacrificing the porosity of MOFs, also allowing the encapsulation of large molecule MOFs. The synthesis of MOFs involves reaction conditions and simple methods such as solvothermal, ionothermal, diffusion, microwave methods, ultrasound‐assisted, template‐directed syntheses, and others [2, 3].

An interesting and significant advancement in the field is to combine MOFs with functional nanoparticles, yielding new nanocomposite materials with unparalleled properties and performance. Nano‐MOFs are advantageous over conventional nanomedicines owing to their structural and chemical diversity, high loading capacity, and biodegradability. The final properties are dependent on the particle composition, size, and morphology. These can be obtained as either crystalline or amorphous materials. As soft porous crystals, framework flexibility (triggered by an external stimulus, e.g., mechanical stress, temperature, light interactions) may be shown by MOFs, also in the absence of guests or with no involvement of adsorption and desorption [13, 16].

Figure 2.

Some examples of organic ligands with carboxylic functionality used for the preparation of MOFs.

Figure 3.

Some examples of ligands containing nitrogen, sulfur, phosphorous and heterocycles used for the preparation of MOFs.

Figure 4.

MOFs resulting from different metal nodes and bridging ligands.

3. Metal biomolecule frameworks (BioMOFs)

Biomolecules are naturally and abundantly available. They are cost‐effective, rigid, and flexible with different coordination sites, rendering structurally diverse, biologically compatible MOFs. MOFs have also been synthesized from nontoxic endogenous cations (such as Ca, Mg, Fe, and Zn) and ligands consisting of naturally occurring derivatives or biomolecules [17]. These BioMOFs are usually biocompatible and suitable for biomedical applications [1747]. Such combinations of natural ligands with endogenous cations are also associated with several therapeutic effects (anti‐allergic, anti‐inflammatory, antimicrobial, anticarcinogenic activities). Table 2 shows some examples of BioMOFs and their applications [1847]. Such biologically and environmentally compatible MOFs are designed and constructed based on specific composition criteria governed by judiciously selecting metal ions and organic linkers as building blocks, which are nontoxic and biologically and environmentally compatible. Biomolecules such as amino acids, peptides, proteins, nucleobases, carbohydrates, and other natural products such as cyclodextrins, porphines, and some carboxylic acids (Figure 5) serve as emerging building blocks for the design and construction of metal‐biomolecule frameworks with novel and interesting properties and applications that cannot be obtained through the use of traditional organic linkers [17, 43, 44, 48, 49].

AplicationBioMOFMetalLigandYear  AuthorRf
Ar and CH4 sorption[Cu(trans‐fum)]CuFum:Fumaric acid2001K. Seki et al
Reversible H2O
NiSuc: Succinic
2002Forster et al.
NiSuc2003Guillou et al.
Sorption of more
than 30 kinds of
guests (e.g. DMF,
structural change
MnFormic acid2004Wang et al.
Selective CO2
and H2 sorption
2004Dybtsev et al.
FeFum2004Serre et al.
NiAmino acid L‐Asp:l‐aspartic acid2004Anokhina et al.
separation and
Znbdc: 1,4‐
acid and L‐
lac:Lactic acid
2006Dybtsev et al.
CO2 sorption[Ni2(L‐Asp)2
NiL‐Asp and
4,4′‐bipy : 1,2‐bis
et al. [26]
H2 sorptionCo2(L‐Asp)2
CoL‐Asp and 4,4′
2008Zhu et al.
catalysts for
the methanolysis
of rac‐propylene
NiL‐Asp and 4,
et al. [28]
catalysts for
the methanolysis
of rac‐propylene
and bpe: 1,2‐bis(4‐
et al. [28]
Cation exchange
cationic drugs
and lanthanide
and bpdc:
2009An et al.
CO2. sorption
·2DMF· 0.5H2O
CoAde2010An et al.
Drug delivery
and imaging
MeOH and [Fe3O(MeOH)(C6H4O8)3Cl]·6MeOH
Fumarate and C6H4O8
is galactarate
et al. [31]
Therapeutic agentBioMIL-1FeNicotinic acid (pyridine-3-carboxylic acid, also called niacin or vitamin B3)2010Miller et al.
flexible structure;
CO2, MeOH and
H2O sorption
2010Rabone et al.
γ ‐CD: cyclodextrins
2010Smaldone et al.
Inclusion of
several molecules
(e.g. Rhodamine B,
γ‐CD is a (chiral) cyclic
composed of
2010Smaldone et al.
Highly selective
adsorption of CO2
CD‐MOF‐2Rbγ‐CD2011Jeremiah J.
Gassensmith et al.
Photostable O2
O·2Me2NH2] loaded
with lanthanide
cations( Tb(III),
Sm(III), Eu(III)
and Yb(III))
Zn and
Ade and bpdc2011An et al.
Fe, Mn, Co
and Ni
H4gal: gallic
2011Saines et al.
comprised of
portrayed in
their stable
4C1 conformations
et al. [38]
and CD‐MOF‐2
K, Rb and Csγ‐CD2012Forgan et al.
Drug storage
and release
or for the
and organization
of large biomolecules
Bio‐MOF‐100ZnAde2012Jihyun An
et al. [40]
MIL‐151 to ‐154ZrH4gal2014Cooper et al.
AntibacterialBioMIL‐5ZnAzA: azelaic
et al. [42]
Mg(H4gal)MgH4gal2015Cooper et al.
Inclusion and
loading the
drug molecules
2015Lu et al.
MOF‐525ZrH4tcpp: meso‐tetra
2015Kung et al.
Ammonia uptakeAl‐PMOFAlH4tcpp2015Wilcox et al.
Highly active
[Zn(ain)(atz)]nZnHatz : 5‐
and Hain: 2‐
2016David Briones
et al. [47]

Table 2.

Some examples of BioMOFs and their applications.

Figure 5.

Examples of organic linkers used for the synthesis of BioMOFs.

4. Summary

MOFs find versatile applications as drug‐delivery agents, sensors, storage and separation systems, catalysts, and others. Nontoxic nano‐MOFs bearing tailored cores and surfaces can be used as nanodrug carriers for antitumor and anti‐HIV drugs (biomedicine, nontoxic, drug). MOFs with biomolecules as organic linkers are still in cradle stage in contrast to their counterparts bearing traditional organic linkers. However, biomolecules confer biological compatibility and easy recyclability to MOFs. They also confer unique characteristics such as chirality and specific recognition, self‐assembly characteristic, separation, ion exchange, and catalytic properties, also rendering bioinspired structures. In future, a better understanding and control of chemistry and design of MOFs may provide plethora of opportunities towards their structures, properties, and applications in different fields.


Dr Fahmina Zafar is thankful to UGC (New Delhi, India) for Dr DS Kothari Postdoctoral Fellowship, Ref. # F.4/2006(BSR)/13‐986/2013(BSR). The author is also thankful to Prof. Nahid Nishat (Mentor), Inorganic Materials Research Lab, Department of Chemistry, Jamia Millia Islamia (a Central University) New Delhi, India, for her kind support.

© 2016 The Author(s). Licensee IntechOpen. This chapter is distributed under the terms of the Creative Commons Attribution 3.0 License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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Eram Sharmin and Fahmina Zafar (October 12th 2016). Introductory Chapter: Metal Organic Frameworks (MOFs), Metal-Organic Frameworks, Fahmina Zafar and Eram Sharmin, IntechOpen, DOI: 10.5772/64797. Available from:

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