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Volumn 17, Issue 16, 1998, Pages 2655-2668

Heterocyclic systems containing antimony (III) -VIII . Hypervalency by intramolecular 1,5-chelation Sb · · · N in rings RSb [ (CH2) 3] 2NR′ (NR′ = NMe, NBz, NBui) and comparison to analogous compounds of AsIII, BiIII, GeIV and SnIV

Author keywords

Antimony; Coulometry; Cyclic voltammetry; Frontier orbitals; Hypervalency; M ssbauer spectroscopy; NMR

Indexed keywords


EID: 0040681960     PISSN: 02775387     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0277-5387(98)00024-2     Document Type: Article
Times cited : (15)

References (26)
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    • ;
    • (c) Musher, J. I., Angew. Chem., 1969, 81, 68 ; Angew. Chem. Int. Ed. Engl., 1969, 8, 54
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    • Cf an Updated View on The Long-Known Model of Vsepr; Angew
    • Cf an updated view on the long-known model of VSEPR : Gillespie R. J., Robinson E. A. Angew.Chem. 108:1996;539 ; Angew.
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    • The Compound 2(nme\cl 2 ) of Has Been Synthesized as The First Compound of This Class
    • 2) of has been synthesized as the first compound of this class : Jurkschat K., Tzschach A. J. Organomet. Chem. 272:1984;13.
    • (1984) J. Organomet. Chem. , vol.272 , pp. 13
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  • 10
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    • A.). Five of The Sb Compounds 4. The Five As Bi Compounds 3. of Have Been Described in a Previous Paper Br a 5.; (b) the data for the fourteen Sn compounds 2 were taken from Ref
    • a) Five of the Sb compounds 4, the five As, Bi compounds 3, 5 of have been described in a previous paper : Br a, Falke R., Ellner A., Beuter M., Kolb U., Dräger M. Polyhedron. 13:1994;365 ; (b) the data for the fourteen Sn compounds 2 were taken from Ref.
    • (1994) Polyhedron , vol.13 , pp. 365
    • Falke, R.1    Ellner, A.2    Beuter, M.3    Kolb, U.4    Dräger, M.5
  • 11
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    • Much Work Has Also Been Done Previously on The Analogous Compound Series R 2 m\rm [sch 2 ch 2 ] 2 x.(a) M. Ge Dr a =.; (b) M = Sn2 : Tzschach
    • 2X.(a) M = Ge : Dr a. Z. Anorg. Allg. Chem. 423:1976;53 ; (b) M = Sn2 : Tzschach, A.
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    • -[1.41* (d -d (standard) ) ] 29 . Single bond standard distances d (Sb N\O\ Cl\I\C) = 2.13\2.04\2.40\2.74\2.19 . Sum of radii without correction for electronegativity :
    • - [1.41* (d -d (standard) ) ] 29 . Single bond standard distances d (Sb N\O\ Cl\I\C) = 2.13\2.04\2.40\2.74\2.19 . Sum of radii without correction for electronegativity : O'Keeffe, M. and Brese, N. E., J. Am. Chem. Soc., 1991, 113, 3226.
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    • Programcacao(computer Aided Composition of Atomic Orbitals); (b) Program HYPERCHEM : Hyperchem
    • a) ProgramCACAO(Computer Aided Composition of Atomic Orbitals) : Mealli C., Proserpio D.M. J.Chem.Educ. 67:1990;399 ; (b) Program HYPERCHEM : Hyperchem.
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  • 18
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    • ii (eV) \exponent : C (2s -21.40\1.625, 2p -11.40\1.625) ; H (1s -13.60\1.300) ; As (4s -16.22\2.23, 4p -12.16\1.89) ; Cl (3s -26.30\2.183, 3p -14.20\1.733) ; Ge (4s -16.00\2.160, 4p -9.00\1.850) ; N (2s -26.00\1.950, 2p -13.40\1.950) ; S (3s -20.0\2.122, 3p -13.3\1.827) ; Sb (5s -18.80\2.323, 5p -11.70\1.999) ; Sn (5s -16.16\2.120, 5p -8.32\1.820) . Compilation by Barcelona
    • ii (eV) \exponent : C (2s -21.40\1.625, 2p -11.40\1.625) ; H (1s -13.60\1.300) ; As (4s -16.22\2.23, 4p -12.16\1.89) ; Cl (3s -26.30\2.183, 3p -14.20\1.733) ; Ge (4s -16.00\2.160, 4p -9.00\1.850) ; N (2s -26.00\1.950, 2p -13.40\1.950) ; S (3s -20.0\2.122, 3p -13.3\1.827) ; Sb (5s -18.80\2.323, 5p -11.70\1.999) ; Sn (5s -16.16\2.120, 5p -8.32\1.820) . Compilation by : Alvarez, S., Table of Parameters for Extended Hückel Calculations, Barcelona, 1985.
    • (1985) Table of Parameters for Extended Hückel Calculations
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    • a) For a recent concise introduction to cyclic voltammetry see Ch. 9, Oxford University Press, Oxford, New York, Tokyo
    • a) For a recent concise introduction to cyclic voltammetry see : Brett, C. M. A. and Oliveira Brett, A. M., Electrochemistry, Ch. 9, Oxford University Press, Oxford, New York, Tokyo, 1993
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    • Brett, C.M.A.1    Oliveira Brett, A.M.2
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    • (c) for cyclic voltammetry on organic antimony compounds see :
    • (c) for cyclic voltammetry on organic antimony compounds see : Dessy, R. E., Chivers, T. and Kitching, W., J. Am. Chem. Soc., 1966, 88, 467.
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    • ; Takeda
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.