Novel transition metal complexes based on covalently linked DMIT systems

Synthetic Metals

Volumn 120, Issue 1-3, 2001, Pages 1023-1024

  Berridge, R ^a   Bricklebank, N ^a   Allen, D W ^a   Skabara, P J ^a,d   Malik, K M A ^b   Coles, S J ^c   Hursthouse, M B ^c  

^a SHEFFIELD HALLAM UNIVERSITY   (United Kingdom)

^b CARDIFF UNIVERSITY   (United Kingdom)

^c UNIVERSITY OF SOUTHAMPTON   (United Kingdom)

^d UNIVERSITY OF MANCHESTER   (United Kingdom)

Author keywords

Heterocycle synthesis; Organic conductors based on radical cation and or anion salts

Indexed keywords

CRYSTALLIZATION; MOLECULAR DYNAMICS; MOLECULAR STRUCTURE; NEGATIVE IONS; PHASE TRANSITIONS; POSITIVE IONS; REDOX REACTIONS; SALTS; SYNTHESIS (CHEMICAL);

ELECTROCRYSTALLIZATION; HETEROCYCLE SYNTHESIS; TRANSITION METAL LIGANDS;

ORGANIC CONDUCTORS;

EID: 0035867286     PISSN: 03796779     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0379-6779(00)01076-6     Document Type: Article

References (5)

1. P. Cassoux, Coord. Chem. Rev. 185-186 (1999) 213.
2. N. Svenstrup, K. M. Rasmussen, T. K. Hansen, J. Becher, Synthesis (1994) 809.
3. 1 = 0.0430 [I>2σI] and 0.1251 and 0.0534 respectively for all data. Deposition number; CCDC 147053.
4. D. Sellmann, J. Sutter, Acc. Chem. Res. 30 (1997) 460.
5. 6 supporting electrolyte (0.1 M) in DMF.