1,1′-Binaphthyl-2,2′-diol and 2,2′-diamino-1,1′-binaphthyl:: versatile frameworks for chiral ligands in coordination and metallosupramolecular chemistry

被引:155
|
作者
Telfer, SG
Kuroda, R
机构
[1] JST ERATO Kuroda Chiromorphol Project, Meguro Ku, Tokyo 1530041, Japan
[2] Univ Tokyo, Grad Sch Arts & Sci, Meguro Ku, Tokyo 1538902, Japan
关键词
binaphthyl ligands; chiral metal complexes; supramolecular chemistry; asymmetric catalysis; nitrogen ligands; oxygen ligands;
D O I
10.1016/S0010-8545(03)00026-2
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
This review covers the use of chiral 1,1'-binaphthyl-2,2'-diol and 2,2'-diamino-1,1'-binaphthyl frameworks for the construction of ligands for coordination and metallosupramolecular chemistry. The 1,1'-binaphthyl-2,2'-diol unit is readily functionalised with ligating groups at both the diol oxygen atoms and at a variety of positions on the binaphthyl rings. This has allowed the synthesis of a wide range of ligands which, in combination with metal ions, has given rise to an array of chiral coordination compounds and supramolecular complexes. This review details polynuclear complexes prepared in this manner. 2,2'-Diamino-1,1'-binaphthyl has been used as a ligand in a number of complexes. Also, ligating groups have been attached to the 2,2-diamino-1,1'-binaphthyl framework via its amine nitrogen atoms, usually by formation of a Schiff base. The coordination chemistry of both the parent 2,2'diamino-1,1'-binaphthyl compound and of its derivatives are covered by this review. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:33 / 46
页数:14
相关论文
共 50 条
  • [41] Di-tert-butyl (1,1′-binaphthyl-2,2′-dioxy)diacetate
    Mustafa, Asra
    Shah, Muhammad Raza
    Khatoon, Maimoona
    Ng, Seik Weng
    ACTA CRYSTALLOGRAPHICA SECTION E-STRUCTURE REPORTS ONLINE, 2009, 65 : O912 - U3313
  • [42] Enantioseparation of racemic 1,1′-binaphthyl-2,2′-diamine by preparative liquid chromatography
    Ryoo, JJ
    Kwon, WJ
    Kim, TH
    Lee, KP
    Choi, SH
    BULLETIN OF THE KOREAN CHEMICAL SOCIETY, 2004, 25 (09) : 1336 - 1340
  • [43] (R)-(+)-2.2′-diamino-1,1′-binaphthyl
    Jones, MD
    Paz, FAA
    Davies, JE
    Johnson, BFG
    ACTA CRYSTALLOGRAPHICA SECTION E-STRUCTURE REPORTS ONLINE, 2003, 59 : O910 - O912
  • [44] (R)-2,2 '-Bis(methoxymethoxy)-1,1 '-binaphthyl
    Zhou, Liang
    Eli, Wumanjiang
    ACTA CRYSTALLOGRAPHICA SECTION E-CRYSTALLOGRAPHIC COMMUNICATIONS, 2012, 68 : O1361 - +
  • [45] Enantioselective Fluorescent Recognition by Using a 1,1′-Binaphthyl-2,2′-diamine Derivative
    Wang, Chao
    Wu, Elaine
    Pu, Lin
    EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, 2017, 2017 (32) : 4736 - 4739
  • [46] (R)-(+)-2,2′-bis(diphenylphosphinoyl)1,1′-binaphthyl
    Bunten, KA
    Farrar, DH
    Lough, AJ
    ACTA CRYSTALLOGRAPHICA SECTION C-CRYSTAL STRUCTURE COMMUNICATIONS, 2000, 56 : E267 - E267
  • [47] (S)-2,2′-bis(dicyclohexylphosphinoamino)-1,1′-binaphthyl
    Guo, RW
    Wang, LL
    Wu, J
    Choi, MCK
    Zhou, ZY
    ACTA CRYSTALLOGRAPHICA SECTION E-CRYSTALLOGRAPHIC COMMUNICATIONS, 2002, 58 : O598 - O599
  • [48] (R)-(+)-2,2'-BIS(DIPHENYLPHOSPHINO)-1,1'-BINAPHTHYL AND (S)-(-)-2,2'-BIS(DIPHENYLPHOSPHINO)-1,1'-BINAPHTHYL (BINAP) - (PHOSPHINE, [1,1'-BINAPHTHALENE]-2,2'-DIYLBIS[DIPHENYLPHOSPHINO, (R)- OR (S)-)
    TAKAYA, H
    AKUTAGAWA, S
    NOYORI, R
    ORGANIC SYNTHESES, 1989, 67 : 20 - 32
  • [49] Enantiopure Chiral Macrocyclic Lanthanide Complexes Derived from (R)-2,2′-Diamino-1,1′-binaphthyl and 2,6-Diformylpyridine
    Jerzy Lisowski
    Marta Paluch
    Tadeusz Lis
    Journal of inclusion phenomena and macrocyclic chemistry, 2006, 55 : 123 - 129
  • [50] Racemization barriers of 1,1′-binaphthyl and 1,1′-binaphthalene-2,2′-diol:: A DFT study
    Meca, L
    Reha, D
    Havlas, Z
    JOURNAL OF ORGANIC CHEMISTRY, 2003, 68 (14): : 5677 - 5680