MODELS FOR THE PHOTOSYNTHETIC REACTION-CENTER - PREPARATION, SPECTROSCOPY, AND CRYSTAL-STRUCTURES AND MOLECULAR-STRUCTURES OF COFACIAL BISPORPHYRINS LINKED BY CIS-1,2-ETHENE AND TRANS-1,2-ETHENE BRIDGES AND OF 1,1-CARBINOL-BRIDGED BISPORPHYRINS

被引:68
作者
SENGE, MO
VICENTE, MGH
GERZEVSKE, KR
FORSYTH, TP
SMITH, KM
机构
[1] Department of Chemistry, University of California, Davis
关键词
D O I
10.1021/ic00103a006
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The low-valent titanium induced reductive coupling of metal(II) 5-formyl-octaethylporphyrin (OEP) (2, 3) leads to the formation of ethene-bridged bisporphyrins. Structural studies on the main products of the coupling of Cu(II) (2) and Ni(II) 5-formyl-OEP (3) revealed, surprisingly, the formation of the cis-isomers 1,2-bis[5-(2,3,7,8,12,13,17,18-octaethylporphyrinato)metal(II)]-cis-ethene (4, 5). This is in contrast to other reported reductive couplings of aldehydes and ketone which usually lead to the trans-product. The cis-isomer can undergo an acid-catalyzed isomerization to the trans-isomer (6, 7) which is also formed as a side product in the coupling reaction. An explanation for the formation of the cis-ethene-bridged bisporphyrins may involve the strong aggregation tendencies of metalloporphyrins. These aggregation forces are evidenced in the crystal structures of the cis-dimers which exhibit considerable overlap of the pi-systems and have a cofacial macrocycle arrangement with almost coplanar macrocycles. Besides the strong intramolecular aggregation effects, intermolecular pi-stacking was observed in the structures of the Cu(II) (4) and Ni(II) (5) cis-dimers, the nickel(II) trans-isomer (7) and the related structure of bis[2-(3,7,8,12,13,17,18-heptaethylpophyrinato)nickel(II)]hydroxymethane (13) which is obtained by low valent titanium coupling of Ni(II) 2-formyl-OEP (12). The synthesis of the cofacial cis-dimers is achieved in a single step from the corresponding formylporphyrins in high yields, thus presenting an improvement over other published procedures for synthesis of face-to-face bisporphyrins. Crystal data: 4, Mo K alpha (lambda = 0.710 69 Angstrom) at 130 K, a = 19.208(7) Angstrom, b = 14.672(5) Angstrom, c = 24.170(7) Angstrom, beta = 111.15(3)degrees, V = 6352(4) Angstrom(3), Z = 4, space group P2(1)/n, R = 0.056; 5, Mo K alpha (lambda = 0.710 69 Angstrom) at 130 K, a = 21.671(7) Angstrom, b = 14.079(5) Angstrom, c = 22.110(7) Angstrom, beta = 108.86(2)degrees, V = 6384(3) Angstrom(3), Z = 4, space group P2(1)/c, R = 0.064; 7, Cu K alpha (lambda = 1.541 78 Angstrom) at 126 K, a = 11.163(3) Angstrom, b = 12.775(4) Angstrom, c = 14.554(3) Angstrom, alpha = 69.59(2)degrees, beta = 81.15(2)degrees, gamma = 73.21(2)degrees, V = 1859(1) Angstrom(3), Z = 1, space group P $($) over bar$$ 1, R = 0.072; 13, Mo K alpha (lambda = 0.710 69 Angstrom) at 130 K, a = 40.31(2) Angstrom, b = 14.997(7) Angstrom, c = 21.954(11) Angstrom, beta = 108.6(4)degrees, V = 12579(10) Angstrom(3), Z = 8, space group C2/c, R = 0.122.
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页码:5625 / 5638
页数:14
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