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Three Novel Copper–Radical Complexes: Syntheses, Crystal Structures, and Magnetic Properties
Author(s) -
Chen Xiaodan,
Rong Rong,
Wang Yun,
Zhu Lili,
Zhao Qihua,
Ang Siau Gek,
Sun Baiwang
Publication year - 2010
Publication title -
european journal of inorganic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.667
H-Index - 136
eISSN - 1099-0682
pISSN - 1434-1948
DOI - 10.1002/ejic.201000005
Subject(s) - chemistry , copper , radical , antiferromagnetism , pyridine , ferromagnetism , crystallography , nitroxide mediated radical polymerization , crystal structure , ion , ligand (biochemistry) , inorganic chemistry , photochemistry , medicinal chemistry , organic chemistry , radical polymerization , biochemistry , physics , receptor , quantum mechanics , copolymer , condensed matter physics , polymer
Abstract Three novel copper–radical complexes [Cu(PhCOO) 2 (NITpPy) 2 (H 2 O) 2 ] ( 1 ), [Cu 2 (Me 3 CCOO) 4 (NITpPy) 2 ] ( 2 ), and [{Cu 2 (Me 3 CCOO) 4 (NITpPy)} n ] ( 3 ) [NITpPy = 4,4,5,5‐tetramethyl‐2‐(4‐pyridyl)‐2‐imidazoline‐1‐oxyl 3‐oxide] were synthesized and characterized structurally as well as magnetically. It is noteworthy that the syntheses of complexes 2 and 3 are similar except for the temperature of the reaction between Cu(Me 3 CCOO) 2 · 2H 2 O and the NITpPy radical ligand. Our magnetic study of complexes 1 and 2 reveals that the antiferromagnetic interactions occur with a J value around –10 cm –1 between copper(II) and radicals when radicals use the pyridine nitrogen atom connected to the copper(II) ion. Yet the best‐fit parameters of complex 3 reveal that significant ferromagnetic interactions ( J 2 = 20.5 cm –1 ) take place in the copper radical when radicals coordinate the copper(II) ion with nitroxide directly.

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