Synthesis and characterization of unsymmetrically tetrasubstituted porphyrin and their nickel (II) complexes with the crystal structure of 5,15-bis(4-aminophenyl)-10, 20-diphenylporphyrinatonickel(II)

被引:20
作者
Hayvali, M
Gündüz, H
Gündüz, N
Kiliç, Z
Hökelek, T [1 ]
机构
[1] Hacettepe Univ, Dept Phys, TR-06532 Ankara, Turkey
[2] Ankara Univ, Dept Chem, TR-06100 Ankara, Turkey
关键词
porphyrins; unsymmetric tetrasubstituted porphyrins; porphyrin-Schiff bases; porphyrin complexes; crystal structure of porphyrin;
D O I
10.1016/S0022-2860(00)00417-8
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
New unsymmetrically tetrasubstituted porphyrin-Schiff base ligands (8-10) containing recognition sites for alkali and transition metal quest cations have been synthesized by the condensations of 5-(4-aminophenyl)-10,15,20- triphenylporphyrin (5) with salycylaldehyde, 2-hydroxy-1-naphthaldehyde and 4'-hydroxy-5'-formyl-benzo-15-crown-5. Homonuclear crystalline 1:1 [Ni(II): ligand] complexes (8a-10a) of the ligands with Ni(CH2COO)(2). 4H(2)O have been obtained. The porphyrin ligands and their complexes have been characterized by elemental analysis, IR, UV-VIS, H-1, C-13 NMR and MS, and the structure of trans-5,15-bis(4-aminophenyl)-10,20-diphenylporphyrinato-nickel(II) (7a) has been examined crystallographically. It crystallizes in the monoclinic space group C2/c with a = 22.096(2), b = 13.455(1), c = 15.599(1) Angstrom, beta = 134.81(1)degrees, V = 3290.6(2) Angstrom(3), Z = 4 and D-x = 1.42 g cm(-3). The molecule is centrosymmetric and the porphine nucleus is non-planar. The average value for the diameter of the hole has been estimated as 3.830(4) Angstrom. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:215 / 226
页数:12
相关论文
共 45 条
[1]  
[Anonymous], 1974, INT TABLES XRAY CRYS, VIV
[2]   PORPHYRINS .7. SYNTHESIS OF PORPHYRINS BY ROTHEMUND REACTION [J].
BADGER, GM ;
LASLETT, RL ;
JONES, RA .
AUSTRALIAN JOURNAL OF CHEMISTRY, 1964, 17 (09) :1028-+
[3]   CONCERNING MESO-TETRAPHENYLPORPHYRIN PURIFICATION [J].
BARNETT, GH ;
HUDSON, MF ;
SMITH, KM .
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 1975, (14) :1401-1403
[4]  
CALWERLEY MJ, 1982, ACTA CHEM SCAND B, V36, P241
[5]   SYNTHESIS OF CROWN-ETHER PRECOCENES [J].
CAMPS, F ;
COLL, J ;
RICART, S .
JOURNAL OF HETEROCYCLIC CHEMISTRY, 1983, 20 (01) :249-250
[6]   SYNTHESIS AND CHARACTERIZATION OF A CROWN-ETHER SUBSTITUTED SALICYLALDIMINE SCHIFF-BASE LIGAND AND ITS COMPLEXES WITH COBALT(II), COPPER(II), NICKEL(II), AND URANYL(VI) [J].
CAN, S ;
BEKAROGLU, O .
JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS, 1988, (11) :2831-2835
[7]  
DIESENHOFER J, 1984, J MOL BIOL, V180, P385
[8]   Self-assembly of a multi-porphyrin supramolecular macrocycle by hydrogen bond molecular recognition [J].
Drain, CM ;
Russell, KC ;
Lehn, JM .
CHEMICAL COMMUNICATIONS, 1996, (03) :337-338
[9]   COMPARISON OF REACTION CENTERS FROM RHODOBACTER-SPHAEROIDES AND RHODOPSEUDOMONAS-VIRIDIS - OVERALL ARCHITECTURE AND PROTEIN-PIGMENT INTERACTIONS [J].
ELKABBANI, O ;
CHANG, CH ;
TIEDE, D ;
NORRIS, J ;
SCHIFFER, M .
BIOCHEMISTRY, 1991, 30 (22) :5361-5369
[10]  
FAIR CK, 1990, MOLEN INTERACTIVE IN