Metal ligand aromatic cation-π interactions

被引:85
作者
Zaric, SD
机构
[1] Univ Belgrade, Dept Chem, YU-11001 Belgrade, Serbia
[2] Free Univ Berlin, Inst Chem, Dept Biol Chem & Pharm, D-14195 Berlin, Germany
关键词
chelates; density functional calculations; DNA; hydrogen bonds; metalloproteins; pi interactions; RNA;
D O I
10.1002/ejic.200200278
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Cation-pi interactions are important noncovalent bonding forces. This review covers a special type of cation-pi interactions, the metal ligand aromatic cation-pi (MLACpi) interaction, where ligands that are coordinated to a metal ion interact with aromatic groups. These interactions have been observed in metalloproteins, metal complexes, biomimetic metal complexes, and when DNA and RNA interact with metal cations. The energy of MLACpi interactions in different systems has been calculated by quantum chemical methods and Was found to vary from 1 to 30 kcal/mol. ((C) Wiley-VCH Verldg GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003).
引用
收藏
页码:2197 / 2209
页数:13
相关论文
共 157 条
[11]   MAGNESIUM BINDING TO THE BACTERIAL CHEMOTAXIS PROTEIN CHEY RESULTS IN LARGE CONFORMATIONAL-CHANGES INVOLVING ITS FUNCTIONAL SURFACE [J].
BELLSOLELL, L ;
PRIETO, J ;
SERRANO, L ;
COLL, M .
JOURNAL OF MOLECULAR BIOLOGY, 1994, 238 (04) :489-495
[12]   Synthesis and characterization of new chiral Schiff base complexes with diiminobinaphthyl or diiminocyclohexyl moieties as potential enantioselective epoxidation catalysts [J].
Bernardo, K ;
Leppard, S ;
Robert, A ;
Commenges, G ;
Dahan, F ;
Meunier, B .
INORGANIC CHEMISTRY, 1996, 35 (02) :387-396
[13]   SYNTHESES, ELECTROCHEMISTRY, AND SPECTROSCOPY OF DIRHODIUM(II) TETRA-ACETAMIDATE AND TETRAKIS(TRIFLUOROACETAMIDE) COMPLEXES WITH AXIAL GROUP-15 SUBSTITUENTS - THE X-RAY CRYSTAL-STRUCTURES OF [RH2(CH3CONH)4(ASPH3)2] AND [RH2(CH3CONH)4-N(CH3CO2)N(ASPH3)2], [RH2(CH3CONH)4-N(CH3CO2)N(SBPH3)2] N ALMOST-EQUAL-TO 1U [J].
BEST, SP ;
CHANDLEY, P ;
CLARK, RJH ;
MCCARTHY, S ;
HURSTHOUSE, MB ;
BATES, PA .
JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS, 1989, (04) :581-588
[14]   CRYSTAL-STRUCTURES OF BIS(2,4-PENTANEDIONATO)BIS(2,6-DIISOPROPYLPHENOXO)TITANIUM(IV), BIS(8-QUINOLINOLATO)BIS(2,6-DIISOPROPYLPHENOXO)TITANIUM(IV), AND BIS(2-METHYL-8-QUINOLINOLATO)BIS(2,6-DIISOPROPYLPHENOXO)TITANIUM(IV) [J].
BIRD, PH ;
FRASER, AR ;
LAU, CF .
INORGANIC CHEMISTRY, 1973, 12 (06) :1322-1328
[15]  
BIRD PH, 1982, ACTA CRYSTALLOGR B, V38, P1586
[16]  
BIYUSHKIN VN, 1991, KOORDINATS KHIM+, V17, P1115
[17]  
Bogdanovic GA, 2002, EUR J INORG CHEM, P1599
[18]   PREPARATION OF OCTAHEDRAL HYDRIDO-AQUO-RUTHENIUM(II) COMPLEXES, AND STRUCTURAL CHARACTERIZATION OF HYDRIDOAQUODICARBONYLBIS(TRIPHENYLPHOSPHINE)-RUTHENIUM(II) TETRAFLUOROBORATE [J].
BONIFACE, SM ;
CLARK, GR ;
COLLINS, TJ ;
ROPER, WR .
JOURNAL OF ORGANOMETALLIC CHEMISTRY, 1981, 206 (01) :109-117
[19]   X-H---π (X = O, N, C) Hydrogen bonds in organometallic crystals [J].
Braga, D ;
Grepioni, F ;
Tedesco, E .
ORGANOMETALLICS, 1998, 17 (12) :2669-2672
[20]   Cation-π interaction in a folded polypeptide [J].
Burghardt, TP ;
Juranic, N ;
Macura, S ;
Ajtai, K .
BIOPOLYMERS, 2002, 63 (04) :261-272