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Chemistry - A European Journal

Volumn 16, Issue 37, 2010, Pages 11250-11253

The use of tethered addends to decrease the number of isomers of bisadduct analogues of PCBM

(2) Bouwer, Ricardo K M a,b Hummelen, Jan C a

a UNIVERSITY OF GRONINGEN (Netherlands)

b DUTCH POLYMER INSTITUTE DPI (Netherlands)

Author keywords

Donor acceptor systems; Fullerenes; Organic solar cells; Regioselectivity; Synthesis design

Indexed keywords

BIS-ADDUCTS; BULK HETEROJUNCTION; BUTYRIC ACIDS; DONOR-ACCEPTOR SYSTEM; METHYL ESTERS; ORGANIC PHOTOVOLTAIC DEVICES; ORGANIC SOLAR CELL; SYNTHESIS DESIGN;

ESTERS; ETHYLENE; ETHYLENE GLYCOL; FATTY ACIDS; FULLERENES; HETEROJUNCTIONS; ISOMERS; SOLAR CELLS;

REGIOSELECTIVITY;

EID: 77957191946 PISSN: 09476539 EISSN: 15213765 Source Type: Journal
DOI: 10.1002/chem.201000537 Document Type: Article

Times cited : (24)

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- Only the trans-1 isomer with both phenyl groups pointing in the same direction shows one resonance for the bridgehead carbon atoms due to Cs symmetry caused by the mirror plane through both addends.

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