메뉴 건너뛰기




Volumn 692, Issue 13, 2007, Pages 2729-2735

Synthesis and structures of polychalcogenadistannabicyclo[k.l.m]alkanes

Author keywords

Polychalcogenadistannabicyclo k.l.m alkanes; Selenium; Sulfur; Tin

Indexed keywords

BOND LENGTH; CHALCOGENIDES; HEXANE; MOLECULAR STRUCTURE; SELENIUM; SULFUR; SYNTHESIS (CHEMICAL);

EID: 34248391331     PISSN: 0022328X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jorganchem.2007.02.004     Document Type: Article
Times cited : (38)

References (53)
  • 2
    • 0001267518 scopus 로고    scopus 로고
    • Abel E.W., Stone F.G.A., and Wilkinson G. (Eds), Pergamon Press, New York
    • Davies A.G. In: Abel E.W., Stone F.G.A., and Wilkinson G. (Eds). Comprehensive Organometallic Chemistry II vol. 2 (1996), Pergamon Press, New York 293
    • (1996) Comprehensive Organometallic Chemistry II , vol.2 , pp. 293
    • Davies, A.G.1
  • 23
    • 0001212301 scopus 로고
    • Pentastanna[1.1.1]propellane derivatives (M, Ch = Sn), see:
    • Pentastanna[1.1.1]propellane derivatives (M, Ch = Sn), see:. Sita L.R., and Kinoshita I. J. Am. Chem. Soc. 111 (1989) 6454
    • (1989) J. Am. Chem. Soc. , vol.111 , pp. 6454
    • Sita, L.R.1    Kinoshita, I.2
  • 27
    • 0000627664 scopus 로고    scopus 로고
    • For recent reviews of the application of m-terphenyl ligands to the synthesis of main group element compounds, see:
    • For recent reviews of the application of m-terphenyl ligands to the synthesis of main group element compounds, see:. Power P.P. Chem. Rev. 99 (1999) 3463
    • (1999) Chem. Rev. , vol.99 , pp. 3463
    • Power, P.P.1
  • 30
    • 9644289203 scopus 로고    scopus 로고
    • For recent examples of the synthesis of compounds of Group 14 elements having unique structures by using m-terphenyl ligands, see:
    • For recent examples of the synthesis of compounds of Group 14 elements having unique structures by using m-terphenyl ligands, see:. Saito M., Tokitoh N., and Okazaki R. J. Am. Chem. Soc. 126 (2004) 15572
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 15572
    • Saito, M.1    Tokitoh, N.2    Okazaki, R.3
  • 38
    • 1242284490 scopus 로고    scopus 로고
    • Activation of elemental sulfur with triethylamine has been demonstrated in several reports, see:
    • Activation of elemental sulfur with triethylamine has been demonstrated in several reports, see:. Terzis A., and Ioannou P.V. Z. Anorg. Allg. Chem. 630 (2004) 278
    • (2004) Z. Anorg. Allg. Chem. , vol.630 , pp. 278
    • Terzis, A.1    Ioannou, P.V.2
  • 42
    • 34248379884 scopus 로고    scopus 로고
    • note
    • 3 were observed at the range from 293 to 330 K, a single resonance was observed at about -31 ppm, suggesting that isomerization between trans and cis isomers should not occur, although the possibility of rapid isomerization between them on the NMR time scale is not completely excluded.
  • 43
    • 0004063249 scopus 로고    scopus 로고
    • 3 are 4404 and 2748 Hz, respectively, see:, VCH, Weinheim p. 243
    • 3 are 4404 and 2748 Hz, respectively, see:. Davies A.G. Organotin Chemistry (1997), VCH, Weinheim p. 243
    • (1997) Organotin Chemistry
    • Davies, A.G.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.