Cu2{[18]ane-N6} complexes:: Structures, magnetism, and phosphate monoester binding

被引:14
作者
Barker, Julia E.
Liu, Yu
Yee, Gordon T.
Chen, Wei-Zhong
Wang, Guangbin
Rivera, Vilma M.
Ren, Tong [1 ]
机构
[1] Univ Miami, Dept Chem, Coral Gables, FL 33124 USA
[2] Virginia Polytech Inst & State Univ, Dept Chem, Blacksburg, VA 24061 USA
[3] Purdue Univ, Dept Chem, W Lafayette, IN 47907 USA
关键词
TETRANUCLEAR COPPER(II) COMPLEX; CRYSTAL-STRUCTURE; SUPRAMOLECULAR CATALYSIS; MACROCYCLIC POLYAMINES; ANION-BINDING; X-RAY; INORGANIC OXOANIONS; PHOSPHORYL TRANSFER; CU(II) COMPLEXES; ATP-HYDROLYSIS;
D O I
10.1021/ic0611140
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
A novel Cu-2(II) complex of the [18] ane-N-6 macrocycle ([18]ane-N-6 = 1,4,7,10,13,16-hexaazacyclooctadecane) was prepared from the reaction between [18] ane-N-6 and Cu-II salts such as Cu(NO3)(2) and Cu(OAc)(2). A structural study of the complex derived from Cu(OAc)(2) (1) revealed a Cu-2(II) core encircled by a [18]ane-N-6 ligand and two mu-O-OAc ligands. The facile replacement of mu-O-OAc by a phosphate monoester [PO3(OR)(2-)] yielded a number of bis(phosphate monoester) dicopper complexes with ROPO32- as hydrogen phosphate (HPO42-, 3a), phenyl phosphate [PO3(OPh)(2-), 3b], glycerol 2-phosphate [PO3(OCH(CH2OH)(2))(2-), 3c], R-D-gluocose phosphate [PO3(C6H11O6)(2-), 3d], and DL-alpha-glycerol phosphate [PO3(OCH2CHOHCH2OH)(2-), 3e]. Structural studies of compounds 3a-d confirmed both the retention of the Cu-2{[18] ane-N-6} core and a mu-O-PO3(OR) coordination mode. Displacement of acetate by a phosphate monoester in an aqueous solution was accompanied by a significant change in the visible absorption, which enables the establishment of relative association constants of PO3(OR)(2-) on the order of 10(4) in the unbuffered solution and 103 in the buffered solution (HEPES). Measurement of the magnetic susceptibility of compound 3a over the temperature range of 5-300 K and subsequent modeling revealed a weak antiferromagnetic coupling (J = -1.1 cm(-1)) between two Cu-II centers.
引用
收藏
页码:7973 / 7980
页数:8
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