Linked Life Data

15643491

Source:http://linkedlifedata.com/resource/pubmed/id/15643491

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
2005-1-11
pubmed:abstractText
By considering the structures of many salts derived from extended TTF analogues, relationships between the molecular architecture of the donors with their electrochemical properties and their stacking mode in the salts are presented in this critical review. Three categories of donors corresponding to their extension modes have been considered. Firstly, for linearly extended TTFs the crucial role of the spacer in modifying the electrochemical properties and the packing mode in the salts is presented. Secondly, bidimentional extension of the donors obtained by linking several dithiafulvenyl units on a TTF core led to materials with increased dimensionality. Finally, the last class corresponds to the fusion, directly or across a benzene ring, of TTF frameworks. The former are the base of many salts with metallic behaviour. (148 references.).
pubmed:language
eng
pubmed:journal
pubmed:status
PubMed-not-MEDLINE
pubmed:month
Jan
pubmed:issn
0306-0012
pubmed:author
pubmed:issnType
Print
pubmed:volume
34
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
69-98
pubmed:year
2005
pubmed:articleTitle
Salts of extended tetrathiafulvalene analogues: relationships between molecular structure, electrochemical properties and solid state organisation.
pubmed:affiliation
Groupe Systemes Conjugues Lineaires, CIMMA, UMR-CNRS 6200, 2 Boulevard Lavoisier, 49045 Angers Cedex France. pierre.frere@univ-angers.fr
pubmed:publicationType
Journal Article