GROUND-STATES OF DCNQI-METAL COMPLEXES, (R(1),R(2)-DCNQI)(2)M - (R(1), R(2)=CH3,I,M=AG,CU,LI1-XCUX)

Authors
Citation
K. Hiraki et K. Kanoda, GROUND-STATES OF DCNQI-METAL COMPLEXES, (R(1),R(2)-DCNQI)(2)M - (R(1), R(2)=CH3,I,M=AG,CU,LI1-XCUX), Molecular crystals and liquid crystals science and technology. Section A, Molecular crystals and liquid crystals, 285, 1996, pp. 157-162
Citations number
14
Categorie Soggetti
Crystallography
ISSN journal
1058725X
Volume
285
Year of publication
1996
Pages
157 - 162
Database
ISI
SICI code
1058-725X(1996)285:<157:GODC(->2.0.ZU;2-I
Abstract
The electrical resistance, magnetic susceptibility, H-1- and C-13-NMR measurements have been performed to investigate the ground states of t he metal complexes of DCNQI, (R(1),R(2)-DCNQI)(2)M, where R(1)(R(2)) i s CH3 (Me) or iodine (I) and M is Ag, Cu or Li1-xCux. A new member of DCNQI-M complexes, (DI-DCNQI)(2)Ag, is nonmetallic below room temperat ure and shows a Bonner-Fisher type of susceptibility, of which the val ue is nealy the same as that of (DI-DCNQI)(2)Cu at room temperature. A n antiferromagnetic ordering was found at 5.5K in contrast to the spin -Peierls ground state in the isostructural (DMe-DCNQI)(2)Ag. The alloy systems, (DMe-DCNQI)(2)Li1-xCux, have been studied with an aim at con trol of the electronic state by the doping of Cu into the insulator, ( DMe-DCNQI)(2)Li. For the Cu doping up to x=30%, the systems show the s pin-Peierls transition while the system with x>50% are metallic down t o low temperatures. The (T1T)(-1) of C-13-NMR shows systematic change with doping.