Probing magnetic exchange interactions in molecular magnets: an inclusion compound of a dithiadiazolyl radical

被引:34
作者
Langley, PJ
Rawson, JM
Smith, JNB
Schuler, M
Bachmann, R
Schweiger, A
Palacio, F
Antorrena, G
Gescheidt, G
Quintel, A
Rechsteiner, P
Hulliger, J
机构
[1] Univ Bern, Dept Chem & Biochem, CH-3012 Bern, Switzerland
[2] Univ Cambridge, Dept Chem, Cambridge CB2 1EW, England
[3] Swiss Fed Inst Technol, Phys Chem Lab, Zurich, Switzerland
[4] Univ Zaragoza, CSIC, Inst Ciencia Mat Aragon, E-50009 Zaragoza, Spain
[5] Univ Basel, Inst Phys Chem, CH-4056 Basel, Switzerland
关键词
D O I
10.1039/a901045i
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Go-sublimation of the dithiadiazolyl radical, p-NCC6H4CNSSN2 with the inclusion-forming; host compound perhydrotriphenylene (PHTP) leads to trichroic crystals of the host-guest complex [PHTP-2]. Molecules of 2 are linked through a CN S interaction (ca. 3.03 Angstrom) to form polar chains within the channels of the PHTP host lattice. The host-guest ratio is approximately 5: 1. Pyroelectric and non-linear optic responses indicate that crystals of. [PHTP-2] are macroscopically polar. A combination of variable temperature solid state EPR spectroscopy and magnetic susceptibility measurements are used to probe the electronic properties of[PHTP-2]; whilst [PHTP-2] is paramagnetic, no exchange coupling between neighbouring molecules of 2 within the channels could be established. The implications of these results on the magnetic exchange pathway of the weak ferromagnet, beta-p-NCC6F4CNSSN beta-1, are discussed.
引用
收藏
页码:1431 / 1434
页数:4
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