The bis-linking of tetrathiafulvalene (TTF) to C60: Towards the control of electron transfer between π-donors and C60
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference14 articles.
1. An X-ray crystallographic analysis of a (BEDT-TTF)2C60 charge-transfer complex
2. Crystal Structure of Buckminsterfullerene (C60) Incorporated by a U-Shaped Twin Donor
3. Synthesis of a rigid "ball-and-chain" donor-acceptor system through Diels-Alder functionalization of buckminsterfullerene (C60)
4. Intramolecular Charge Transfer Interaction in 1,3-Diphenyl-2-pyrazoline Ring-Fused C60
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1. Synthesis of glycoluril-tetrathiafulvalene molecular clips for electron-deficient neutral guests through a straightforward Diels–Alder strategy;New J. Chem.;2014-08-26
2. One-pot thermally chemocontrolled double Diels–Alder strategies. A route to [4 + 2] functionalisation/[4 + 2] derivatization of C60;RSC Advances;2013
3. Bis-semiquinone (bi-radical) formation by photoinduced proton coupled electron transfer in covalently linked catechol–quinone systems: Aviram's hemiquinones revisited;Photochemical & Photobiological Sciences;2012
4. Construction and radical cation stabilisation of a supramolecular dyad by tetrathiafulvalene-modified β-cyclodextrin and cucurbit[7]uril;Supramolecular Chemistry;2011-04-15
5. Supramolecular architecture of tetrathiafulvalene-bridged bis(β-cyclodextrin) with porphyrin and its electron transfer behaviors;Photochem. Photobiol. Sci.;2011
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