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Volumn 28, Issue 21, 2009, Pages 6234-6242

Diphenylphosphino- or dicyclohexylphosphino-tethered boryl pincer ligands: Syntheses of PBP Iridium(III) complexes and their conversion to iridium-ethylene complexes

Author keywords

[No Author keywords available]

Indexed keywords

BORON ATOM; COMPLEXATION REACTION; COMPUTATIONAL STUDIES; CYCLOHEXYL; ELECTRON COMPLEXES; HYDRIDE LIGANDS; IRIDIUM COMPLEX; NMR SPECTROSCOPY; PHENYL GROUP; PHOSPHORUS ATOM; PINCER LIGANDS; QUANTITATIVE FORMATION; SPECTRAL CHANGE; STERIC BULK; THEORETICAL CALCULATIONS; X-RAY STRUCTURE;

EID: 70350714274     PISSN: 02767333     EISSN: None     Source Type: Journal    
DOI: 10.1021/om9006455     Document Type: Article
Times cited : (87)

References (90)
  • 25
    • 85013710527 scopus 로고    scopus 로고
    • Morales-Morales, D.; Jensen C. M., Eds.; Elsevier: Oxford
    • The Chemistry of Pincer Compounds; Morales-Morales, D.; Jensen, C. M., Eds.; Elsevier: Oxford, 2007.
    • (2007) The Chemistry of Pincer Compounds
  • 73
    • 0003825713 scopus 로고    scopus 로고
    • NIST Standard Reference Database Number 101 Release 14, Sept Johnson, R. D., III, Ed.
    • Obtained vibration numbers were scaled with a factor of 0.961 for B3LYP/LanL2DZ calculations. See: NIST Computational Chemistry Comparison and Benchmark Database, NIST Standard Reference Database Number 101 Release 14, Sept 2006, Johnson, R. D., III, Ed.; http://srdata.nist.gov/cccbdb.
    • (2006) NIST Computational Chemistry Comparison and Benchmark Database
  • 75
    • 0000033707 scopus 로고
    • 5 complexes has been attributed to the lack of pπ-dπ interaction between two non-π-donor ligands such as hydrides and the central metal by Eisenstein with theoretical calculations. See: (b) Rachidi, I. El-I.; Eisenstein, O.; Jean, Y. New J. Chem. 1990, 14, 671.
    • (1990) New J. Chem. , vol.14 , pp. 671
    • El-I, R.I.1    Eisenstein, O.2    Jean, Y.3
  • 76
    • 0000384893 scopus 로고    scopus 로고
    • So far, it is not clear why the "π-acceptor"' boryl ligand led to a similar geometry
    • (c) Riehl, J. F.; Jean, Y.; Eisenstein, O.; Pelissier, M. Organometallics 2002, 11, 729-737. So far, it is not clear why the "π-acceptor"' boryl ligand led to a similar geometry.
    • (2002) Organometallics , vol.11 , pp. 729-737
    • Riehl, J.F.1    Jean, Y.2    Eisenstein, O.3    Pelissier, M.4
  • 77
    • 0000124143 scopus 로고    scopus 로고
    • It is often said "H is easy to locate through quantum calculations but hard to locate through experimental techniques"; we could believe the location of the hydride ligand generated by calculation rather than X-ray analysis. See: Maseras, F.; Lledos, A.; Clot, E.; Eisenstein, O. Chem. Rev. 2000, 100, 601-636.
    • (2000) Chem. Rev. , vol.100 , pp. 601-636
    • Maseras, F.1    Lledos, A.2    Clot, E.3    Eisenstein, O.4
  • 89
    • 0004150157 scopus 로고    scopus 로고
    • University of Göttingen: Göttingen, Germany
    • Sheldrick, G. M. SHELXL-97; University of Göttingen: Göttingen, Germany, 1997.
    • (1997) SHELXL-97
    • Sheldrick, G.M.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.