Sikdar, Nivedita and Jayaramulu, Kolleboyina and Kiran, Venkayala and Rao, Venkata K and Sampath, Srinivasan and George, Subi J and Maji, Tapas Kumar (2015) Redox-Active Metal-Organic Frameworks: Highly Stable Charge-Separated States through Strut/Guest-to-Strut Electron Transfer. In: CHEMISTRY-A EUROPEAN JOURNAL, 21 (33). pp. 11701-11706.
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Abstract
Molecular organization of donor and acceptor chromophores in self-assembled materials is of paramount interest in the field of photovoltaics or mimicry of natural light-harvesting systems. With this in mind, a redox-active porous interpenetrated metal-organic framework (MOF), {Cd(bpdc)(bpNDI)]4.5H(2)ODMF}(n) (1) has been constructed from a mixed chromophoric system. The -oxo-bridged secondary building unit, {Cd-2(-OCO)(2)}, guides the parallel alignment of bpNDI (N,N-di(4-pyridyl)-1,4,5,8-naphthalenediimide) acceptor linkers, which are tethered with bpdc (bpdcH(2)=4,4-biphenyldicarboxylic acid) linkers of another entangled net in the framework, resulting in photochromic behaviour through inter-net electron transfer. Encapsulation of electron-donating aromatic molecules in the electron-deficient channels of 1 leads to a perfect donor-acceptor co-facial organization, resulting in long-lived charge-separated states of bpNDI. Furthermore, 1 and guest encapsulated species are characterised through electrochemical studies for understanding of their redox properties.
Item Type: | Journal Article |
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Publication: | CHEMISTRY-A EUROPEAN JOURNAL |
Publisher: | WILEY-V C H VERLAG GMBH |
Additional Information: | Copy right for this article belongs to the WILEY-V C H VERLAG GMBH, BOSCHSTRASSE 12, D-69469 WEINHEIM, GERMANY |
Keywords: | electron transfer; host-guest systems; metal-organic frameworks; photochromism; redox-active systems |
Department/Centre: | Division of Chemical Sciences > Inorganic & Physical Chemistry |
Date Deposited: | 03 Sep 2015 05:06 |
Last Modified: | 03 Sep 2015 05:06 |
URI: | http://eprints.iisc.ac.in/id/eprint/52280 |
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