메뉴 건너뛰기




Volumn , Issue 1, 2010, Pages 74-94

Synthesis and characterisation of 2,2-bis(hydroxymethyl)-1,3-diselenolato metal(II) complexes bearing various phosphanes

Author keywords

Hydrogen bonds; Phosphane ligands; Selenolato ligands; Steric demand; X ray diffraction

Indexed keywords

CHELATION; COMPLEXATION; CRYSTAL STRUCTURE; HYDROGEN BONDS; MASS SPECTROMETRY; METAL COMPLEXES; METHANOL; NAPHTHALENE; NICKEL COMPOUNDS; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; PLATINUM COMPOUNDS; SELENIUM COMPOUNDS; SINGLE CRYSTALS; SYNTHESIS (CHEMICAL); X RAY DIFFRACTION;

EID: 74049164243     PISSN: 14341948     EISSN: 10990682     Source Type: Journal    
DOI: 10.1002/ejic.200900824     Document Type: Article
Times cited : (33)

References (126)
  • 72
    • 85163246006 scopus 로고    scopus 로고
    • Due to the presence of heavy atoms, the hydrogen atoms are fixed at calculated positions in all X-ray structures and were not directly determined from the diffraction. Taking the marginal part of the hydrogen atoms in the electron density into account, their positions are not satisfyingly determinable. Hence, the notation of "hydrogen bond" refers to O⋯E (E = N, O, Se, Pt) distances throughout this article and short contacts might be explained by the presence of hydrogen bonds. A conclusion about the O-H⋯E angle cannot be drawn
    • Due to the presence of heavy atoms, the hydrogen atoms are fixed at calculated positions in all X-ray structures and were not directly determined from the diffraction. Taking the marginal part of the hydrogen atoms in the electron density into account, their positions are not satisfyingly determinable. Hence, the notation of "hydrogen bond" refers to O⋯E (E = N, O, Se, Pt) distances throughout this article and short contacts might be explained by the presence of hydrogen bonds. A conclusion about the O-H⋯E angle cannot be drawn.
  • 77
    • 0003699562 scopus 로고    scopus 로고
    • John Wiley & Sons, Ltd, Chichester, New York, Weinheim, Brisbane, Singapore, Toronto
    • J. W. Steed, J. L. Atwood, Supramolecular Chemistry, John Wiley & Sons, Ltd, Chichester, New York, Weinheim, Brisbane, Singapore, Toronto, 2000.
    • (2000) Supramolecular Chemistry
    • Steed, J.W.1    Atwood, J.L.2
  • 84
    • 85163250090 scopus 로고    scopus 로고
    • Litentiate Thesis, University of Oulu, Finland
    • a) M. Risto, Litentiate Thesis, University of Oulu, Finland 2006;
    • (2006)
    • Risto, M.1
  • 103
    • 85163244837 scopus 로고
    • for some examples and reviews on this topic see following and literature cited therein: a) J. C. Jeffrey, T. B. Rauchfuss, Inorg. Chem. 1979, 18, 2858-2866;
    • (1979) Inorg. Chem. , vol.18 , pp. 2858-2866
    • Jeffrey, J.C.1    Rauchfuss, T.B.2
  • 121
    • 0000156087 scopus 로고
    • U. Nagel, Chem. Ber. 1982, 115, 1998-1999.
    • (1982) Chem. Ber. , vol.115 , pp. 1998-1999
    • Nagel, U.1
  • 123
    • 85163243568 scopus 로고    scopus 로고
    • Data Collection Software, Nonius B. V., Netherlands
    • a) COLLECT, Data Collection Software, Nonius B. V., Netherlands, 1998;
    • (1998) Collect
  • 124
    • 0031059866 scopus 로고    scopus 로고
    • Processing of X-ray Diffraction Data Collected in Oscillation Mode
    • Methods in Enzymology (Eds.: C. W. Carter, R. M. Sweet), part A, New York, Academic Press
    • b) Processing of X-ray Diffraction Data Collected in Oscillation Mode: Z. Otwinowski, W. Minor, in: Methods in Enzymology (Eds.: C. W. Carter, R. M. Sweet), vol.276, Macromolecular Crystallography, part A, pp. 307-326, New York, Academic Press, 1997.
    • (1997) Macromolecular Crystallography , vol.276 , pp. 307-326
    • Otwinowski, Z.1    Minor, W.2
  • 126
    • 0004150157 scopus 로고    scopus 로고
    • rel. 97-2, University of Göttingen, Germany
    • G. M. Sheldrick, SHELXL-97 (rel. 97-2), University of Göttingen, Germany, 1997.
    • (1997) SHELXL-97
    • Sheldrick, G.M.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.