Facile anaerobic oxidative dehydrogenation promoted by bases: The case of copper-2,4-dihydro-1H-benzo[d][1,3]oxazine complexes

被引:16
作者
Ardizzoia, G. Attilio [1 ]
Brenna, Stefano [1 ]
Castelli, Fulvio [1 ]
Galli, Simona [1 ]
Masciocchi, Norberto [1 ]
机构
[1] Univ Insubria, Dipartimento Sci Chim & Ambientali, I-22100 Como, Italy
关键词
Copper; Oxidative dehydrogenation; Carbon monoxide; Carbonyl complexes; COPPER; LIGAND; OXAZINE; COORDINATION; BENZOXAZINE; DERIVATIVES; REACTIVITY;
D O I
10.1016/j.ica.2009.10.016
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Two new 2,4-dihydro-1H-benzo[d][1,3]oxazines (L-1 and L-2) were prepared by condensation of 2-quinolinecarboxaldehyde and 2-amino-benzyl alcohols and tested as N,N'-bidentate ligands toward CuCl2. Treatment of the resulting copper(II) derivatives with Et3N promoted an oxidative dehydrogenation yielding the corresponding copper(I) [Cu(L-ox)Cl] complexes, 2, (L-ox = 4H-benzo[d][1,3]oxazine). The [Cu(L-2-ox)Cl] species, 2b, was characterized by single crystal X-ray diffraction, showing a trigonal geometry at the metal center and reacted with PPh3 and CO, affording [Cu(L-2-ox)(PPh3)Cl], 4b, and [Cu(L-2-ox)(CO)Cl], 6b, respectively. The latter species, stable in the solid state, was structurally characterized by diffraction methods and showed tetrahedral coordination of the Cu(I) ion. (C) 2009 Elsevier B. V. All rights reserved.
引用
收藏
页码:324 / 329
页数:6
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