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Stoichiometry-Controlled Two Flexible Interpenetrated Frameworks: Higher CO2 Uptake in a Nanoscale Counterpart Supported by Accelerated Adsorption Kinetics

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dc.contributor.author Sikdar, Nivedita
dc.contributor.author Hazra, Arpan
dc.contributor.author Maji, Tapas Kumar
dc.date.accessioned 2017-02-21T07:02:06Z
dc.date.available 2017-02-21T07:02:06Z
dc.date.issued 2014
dc.identifier.citation Sikdar, N; Hazra, A; Maji, TK, Stoichiometry-Controlled Two Flexible Interpenetrated Frameworks: Higher CO2 Uptake in a Nanoscale Counterpart Supported by Accelerated Adsorption Kinetics. Inorganic Chemistry 2014, 53 (12) 5993-6002, http://dx.doi.org/10.1021/ic500234r en_US
dc.identifier.citation Inorganic Chemistry en_US
dc.identifier.citation 53 en_US
dc.identifier.citation 12 en_US
dc.identifier.issn 0020-1669
dc.identifier.uri https://libjncir.jncasr.ac.in/xmlui/10572/2420
dc.description Restricted Access en_US
dc.description.abstract Here, we report the synthesis, structural characterizations, and gas storage properties of two new 2-fold interpenetrated 3D frameworks, {[Zn-2(bpdc)(2)(azpy)]center dot 2H(2)O center dot 2DMF}(n) (1) and {[Zn-3(bpdc)(3)(azpy)]center dot 4H2O center dot 2DEF}(n), (2) [bpdc = 4,4'-biphenyldicarboxylate; azpy = 4,4'-azobipyridine], obtained from the same set of organic linkers. Furthermore, 1 has been successfully miniaturized to nanoscale (MOF1N) of spherical morphology to study size dependent adsorption properties through a coordination modulation method. The two different SBUs, dinuclear paddle-wheel {Zn-2(COO)(4)} for 1 and trinuclear {Zn-3(mu(2)-OCO)(2)(COO)(4)}for 2, direct the different network topologies of the frameworks that render different adsorption characteristics into the systems. Both of the frameworks show guest induced structural transformations as supported by PXRD studies. Adsorption studies of 1 and 2 show CO2 selectivity over several other gases (such as ND HD OD and Ar) under identical experimental conditions. Interestingly, MOF1N exhibits significantly higher CO2 storage capacity compared to bulk crystals of 1 and that can be attributed to the smaller diffusion barrier at the nanoscale that is supported by studies of adsorption kinetics in both states. Kinetic measurement based on water vapor adsorption clearly distinguishes between the rate of diffusion of bulk (1) and nanospheres (MOF1N). The respective kinetic rate constant (k, s(-1)) for MOF1N (k = 1.29 X 10(-2) s(-1)) is found to be considerably higher than 1 (k = 7.1 X 10(-3) s(-1)) as obtained from the linear driving force (LDF) model. This is the first account where a new interpenetrated MOF has been scaled down to nanoscale through a coordination modulation method, and their difference in gas uptake properties has been correlated through a higher rate of mass diffusion as obtained from kinetics of adsorption. en_US
dc.description.uri 1520-510X en_US
dc.description.uri http://dx.doi.org/10.1021/ic500234r en_US
dc.language.iso English en_US
dc.publisher American Chemical Society en_US
dc.rights @American Chemical Society, 2014 en_US
dc.subject Inorganic & Nuclear Chemistry en_US
dc.subject Metal-Organic Frameworks en_US
dc.subject Porous Coordination Polymer en_US
dc.subject Crystal-Structure en_US
dc.subject Air Separation en_US
dc.subject Building Units en_US
dc.subject Drug-Delivery en_US
dc.subject Selectivity en_US
dc.subject Sorption en_US
dc.subject Temperature en_US
dc.subject Gases en_US
dc.title Stoichiometry-Controlled Two Flexible Interpenetrated Frameworks: Higher CO2 Uptake in a Nanoscale Counterpart Supported by Accelerated Adsorption Kinetics en_US
dc.type Article en_US


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