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Volumn , Issue 35, 2008, Pages 5439-5454

Coordination chemistry of neutral (Ln)-Z amphoteric and ambiphilic ligands

Author keywords

Ambiphilic ligands; Amphoteric ligands; Bifunctional ligands; Lewis acids

Indexed keywords

ACCEPTOR MOIETIES; AMBIPHILIC LIGANDS; AMPHOTERIC LIGAND; BIFUNCTIONAL LIGAND; CO-ORDINATION CHEMISTRIES; DONOR AND ACCEPTOR; DONOR MOIETY; LEWIS ACID; SELF AGGREGATION;

EID: 57149087058     PISSN: 14341948     EISSN: 10990682     Source Type: Journal    
DOI: 10.1002/ejic.200800784     Document Type: Short Survey
Times cited : (153)

References (131)
  • 3
    • 84889361944 scopus 로고    scopus 로고
    • Eds: K. Mikami, M. Lautens, John Wiley & Sons, Inc, Hoboken, N. J
    • b) M. Shibasaki, M. Kanai in New Frontiers in Asymmetric Catalysis (Eds: K. Mikami, M. Lautens), John Wiley & Sons, Inc., Hoboken, N. J., 2007, pp. 383-410;
    • (2007) New Frontiers in Asymmetric Catalysis , pp. 383-410
    • Shibasaki, M.1    Kanai, M.2
  • 20
    • 85163236782 scopus 로고    scopus 로고
    • While amphoteric indicates that a molecule can act as an acid or a base, which is the case for the class of ligands reported here, ambiphilic provides evidence that these ligands can interact by two distinctive chemical functionalities. The two terms will be used indiscriminately throughout the document.
    • While "amphoteric" indicates that a molecule can act as an acid or a base, which is the case for the class of ligands reported here, "ambiphilic" provides evidence that these ligands can interact by two distinctive chemical functionalities. The two terms will be used indiscriminately throughout the document.
  • 22
    • 0003441992 scopus 로고    scopus 로고
    • H. Yamamoto Ed, Wiley-VCH, Weimheim
    • b) H. Yamamoto (Ed.), Lewis Acids in Organic Synthesis, Wiley-VCH, Weimheim, 2000;
    • (2000) Lewis Acids in Organic Synthesis
  • 54
    • 85163237259 scopus 로고    scopus 로고
    • Few leading reviews: a H. Braunschweig, C. Kollann, D. Rais, Angew. Chem. Int. Ed. 2006, 45, 5254-5274;
    • Few leading reviews: a) H. Braunschweig, C. Kollann, D. Rais, Angew. Chem. Int. Ed. 2006, 45, 5254-5274;
  • 122
    • 85163240348 scopus 로고    scopus 로고
    • [79] the M→Z interaction is formally a -2 ligand, which is in agreement with the activation of the B-H bond which is oxidative in nature. However, as shown in one of the latter sections of the document, experimental evidence is in favour of a M→B interaction being dative in nature, the transition metal keeping its original electronic configuration.
    • [79] the M→Z interaction is formally a -2 ligand, which is in agreement with the activation of the B-H bond which is oxidative in nature. However, as shown in one of the latter sections of the document, experimental evidence is in favour of a M→B interaction being dative in nature, the transition metal keeping its original electronic configuration.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.