Pyrazolate-bridging dinucleating ligands containing hydrogen-bond donors: Synthesis and structure of their cobalt analogues

被引:21
作者
Zinn, PJ
Powell, DR
Day, VW
Hendrich, MP
Sorrell, TN [1 ]
Borovik, AS
机构
[1] Univ N Carolina, Chapel Hill, NC 27599 USA
[2] Univ Kansas, Dept Chem, Lawrence, KS 66045 USA
[3] Carnegie Mellon Univ, Pittsburgh, PA 15213 USA
关键词
D O I
10.1021/ic060009n
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Convergent preparative routes to new urea-pyrazolate dinucleating ligands are described. Metal complexes of these ligands have hydrogen bond donors that are proximal to the metal centers that interact with other coordinated species. This is exemplified by Co-II dimers with Co-II-mu-Cl-Co-II motifs, in which the chloro ligand is involved in four intramolecular hydrogen bonds, These noncovalent interactions appear to influence the Coll-Cl bonds, which are unusually long, having lengths greater than 2.5 angstrom.
引用
收藏
页码:3484 / 3486
页数:3
相关论文
共 42 条
[1]   Preparation and structural characterization of a novel dicopper(II) complex with a terminal hydroxide: a structural model of an active site in phosphohydrolases [J].
Arii, H ;
Funahashi, Y ;
Jitsukawa, K ;
Masuda, H .
DALTON TRANSACTIONS, 2003, (11) :2115-2116
[2]   Modeling the active site chemistry of liver alcohol dehydrogenase:: Mononuclear zinc methanol and N,N-Dimethylformamide complexes of a nitrogen/sulfur ligand possessing an internal hydrogen bond donor [J].
Berreau, LM ;
Makowska-Grzyska, MM ;
Arif, AM .
INORGANIC CHEMISTRY, 2001, 40 (10) :2212-+
[3]   Bioinspired hydrogen bond motifs in ligand design: The role of noncovalent interactions in metal ion mediated activation of dioxygen [J].
Borovik, AS .
ACCOUNTS OF CHEMICAL RESEARCH, 2005, 38 (01) :54-61
[4]  
Buchler S, 1999, Z NATURFORSCH B, V54, P1295
[5]   Tunable TACN/pyrazolate hybrid ligands as dinucleating scaffolds for metallobiosite modeling-dinickel(II) complexes relevant to the urease active site [J].
Buchler, S ;
Meyer, F ;
Kaifer, E ;
Pritzkow, H .
INORGANICA CHIMICA ACTA, 2002, 337 :371-386
[6]   CONFORMATIONAL CONTROL OF INTRAMOLECULAR HYDROGEN-BONDING IN HEME MODELS - MAXIMAL CO-II-O-2 BINDING IN A C-CLAMP PORPHYRIN [J].
CHANG, CK ;
LIANG, Y ;
AVILES, G .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1995, 117 (14) :4191-4192
[7]   Large scale ab initio quantum chemical calculation of the intermediates in the soluble methane monooxygenase catalytic cycle [J].
Dunietz, BD ;
Beachy, MD ;
Cao, YX ;
Whittington, DA ;
Lippard, SJ ;
Friesner, RA .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2000, 122 (12) :2828-2839
[8]   Outer sphere mutations perturb metal reactivity in manganese superoxide dismutase [J].
Edwards, RA ;
Whittaker, MM ;
Whittaker, JW ;
Baker, EN ;
Jameson, GB .
BIOCHEMISTRY, 2001, 40 (01) :15-27
[9]  
FULOP V, 1994, STRUCTURE, V2, P201, DOI 10.1016/s0969-2126(00)00021-6
[10]   Activation of the C-H bond of methane by intermediate Q of methane monoozygenase: A theoretical study [J].
Gherman, BF ;
Dunietz, BD ;
Whittington, DA ;
Lippard, SJ ;
Friesner, RA .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2001, 123 (16) :3836-3837