메뉴 건너뛰기




Volumn 636, Issue 1-2, 2001, Pages 17-25

Electronic and steric properties of stable silylene ligands in metal(0) carbonyl complexes

Author keywords

Coordination complexes; Crystal structure; Silylene

Indexed keywords


EID: 0002322588     PISSN: 0022328X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0022-328X(01)00765-3     Document Type: Article
Times cited : (125)

References (34)
  • 1
    • 0347795845 scopus 로고
    • For reviews, see (a) in: S. Patai, Z. Rappoport (Eds.), chap. 24
    • For reviews, see (a) T.D. Tilley, in: S. Patai, Z. Rappoport (Eds.), The Chemistry of Organosilicon Compounds, Wiley, 1989, chap. 24. (b) P.D. Lickiss, Chem. Soc. Rev. (1992) 271. (c) K. H. Pannell, H, K, Sharma, Chem. Rev. (1995) 1351. (d) C. Zybill, Top. Curr. Chem. 160 (1991) 1.
    • (1989) The Chemistry of Organosilicon Compounds
    • Tilley, T.D.1
  • 2
    • 0002003212 scopus 로고
    • (b)
    • For reviews, see (a) T.D. Tilley, in: S. Patai, Z. Rappoport (Eds.), The Chemistry of Organosilicon Compounds, Wiley, 1989, chap. 24. (b) P.D. Lickiss, Chem. Soc. Rev. (1992) 271. (c) K. H. Pannell, H, K, Sharma, Chem. Rev. (1995) 1351. (d) C. Zybill, Top. Curr. Chem. 160 (1991) 1.
    • (1992) Chem. Soc. Rev. , pp. 271
    • Lickiss, P.D.1
  • 3
    • 0347165827 scopus 로고
    • (c)
    • For reviews, see (a) T.D. Tilley, in: S. Patai, Z. Rappoport (Eds.), The Chemistry of Organosilicon Compounds, Wiley, 1989, chap. 24. (b) P.D. Lickiss, Chem. Soc. Rev. (1992) 271. (c) K. H. Pannell, H, K, Sharma, Chem. Rev. (1995) 1351. (d) C. Zybill, Top. Curr. Chem. 160 (1991) 1.
    • (1995) H, K, Sharma, Chem. Rev. , pp. 1351
    • Pannell, K.H.1
  • 4
    • 0001778257 scopus 로고
    • (d)
    • For reviews, see (a) T.D. Tilley, in: S. Patai, Z. Rappoport (Eds.), The Chemistry of Organosilicon Compounds, Wiley, 1989, chap. 24. (b) P.D. Lickiss, Chem. Soc. Rev. (1992) 271. (c) K. H. Pannell, H, K, Sharma, Chem. Rev. (1995) 1351. (d) C. Zybill, Top. Curr. Chem. 160 (1991) 1.
    • (1991) Top. Curr. Chem. , vol.160 , pp. 1
    • Zybill, C.1
  • 5
    • 33746577674 scopus 로고
    • Fischer carbenes exhibit electrophilic behavior in contrast to Schrock carbenes, which are normally nucleophilic. See (a)
    • Fischer carbenes exhibit electrophilic behavior in contrast to Schrock carbenes, which are normally nucleophilic. See (a) E.O. Fischer, A. Massböl, Angew. Chem. Int. Ed. Engl. 3 (1964) 580. (b) K.H. Dotz, E.O. Fischer, P. Hoffmann, F.R. Kreissel, U. Schubert, K. Weiss, Transition Metal Carbene Complexes, Verlag Chemie, 1983.
    • (1964) Angew. Chem. Int. Ed. Engl. , vol.3 , pp. 580
    • Fischer, E.O.1    Massböl, A.2
  • 9
    • 11644310835 scopus 로고
    • See for example (a)
    • See for example (a) D.A. Straus, S.D. Grumbine, T.D. Tilley, J. Am. Chem. Soc. 116 (1994) 7801. (b) S.K. Grumbine, T.D. Tilley, J. Am. Chem. Soc. 116 (1994) 5495.
    • (1994) J. Am. Chem. Soc. , vol.116 , pp. 7801
    • Straus, D.A.1    Grumbine, S.D.2    Tilley, T.D.3
  • 10
    • 11644310835 scopus 로고
    • (b)
    • See for example (a) D.A. Straus, S.D. Grumbine, T.D. Tilley, J. Am. Chem. Soc. 116 (1994) 7801. (b) S.K. Grumbine, T.D. Tilley, J. Am. Chem. Soc. 116 (1994) 5495.
    • (1994) J. Am. Chem. Soc. , vol.116 , pp. 5495
    • Grumbine, S.K.1    Tilley, T.D.2
  • 25
    • 0000122520 scopus 로고    scopus 로고
    • N-heterocyclic silylenes cannot be viewed as true "cones" due to their planar configuration, and may be better described as "fences". See (a)
    • N-heterocyclic silylenes cannot be viewed as true "cones" due to their planar configuration, and may be better described as "fences". See (a) J. Huang, H. Schanz, E.D. Stevens, S.P. Nolan, Organometallics 18 (1999) 2370. (b) T.E. Muller, D.M.P. Mingos, Transition Metal Chem. 20 (1995) 533.
    • (1999) Organometallics , vol.18 , pp. 2370
    • Huang, J.1    Schanz, H.2    Stevens, E.D.3    Nolan, S.P.4
  • 26
    • 0000242318 scopus 로고
    • (b)
    • N-heterocyclic silylenes cannot be viewed as true "cones" due to their planar configuration, and may be better described as "fences". See (a) J. Huang, H. Schanz, E.D. Stevens, S.P. Nolan, Organometallics 18 (1999) 2370. (b) T.E. Muller, D.M.P. Mingos, Transition Metal Chem. 20 (1995) 533.
    • (1995) Transition Metal Chem. , vol.20 , pp. 533
    • Muller, T.E.1    Mingos, D.M.P.2
  • 27
    • 0011712227 scopus 로고
    • Detailed IR studies of analogous carbene complexes can be found in (a)
    • Detailed IR studies of analogous carbene complexes can be found in (a) K. Öfele, M. Herberhold, Z. Naturforsch. 28 (1973) 306. (b) P.B. Hitchcock, M.F. Lappert, P.L. Pye, J. Chem. Soc. Dalton Trans. (1977) 2160. (c) M.F. Lappert, P.L. Pye, G.M. McLaughlin, J. Chem. Soc. Dalton Trans. (1984) 1307. (d) M.F. Lappert, P.L. Pye, J. Chem. Soc. Dalton Trans. (1977) 1283.
    • (1973) Z. Naturforsch. , vol.28 , pp. 306
    • Öfele, K.1    Herberhold, M.2
  • 28
    • 51149210110 scopus 로고
    • (b)
    • Detailed IR studies of analogous carbene complexes can be found in (a) K. Öfele, M. Herberhold, Z. Naturforsch. 28 (1973) 306. (b) P.B. Hitchcock, M.F. Lappert, P.L. Pye, J. Chem. Soc. Dalton Trans. (1977) 2160. (c) M.F. Lappert, P.L. Pye, G.M. McLaughlin, J. Chem. Soc. Dalton Trans. (1984) 1307. (d) M.F. Lappert, P.L. Pye, J. Chem. Soc. Dalton Trans. (1977) 1283.
    • (1977) J. Chem. Soc. Dalton Trans. , pp. 2160
    • Hitchcock, P.B.1    Lappert, M.F.2    Pye, P.L.3
  • 29
    • 0345904519 scopus 로고
    • (c)
    • Detailed IR studies of analogous carbene complexes can be found in (a) K. Öfele, M. Herberhold, Z. Naturforsch. 28 (1973) 306. (b) P.B. Hitchcock, M.F. Lappert, P.L. Pye, J. Chem. Soc. Dalton Trans. (1977) 2160. (c) M.F. Lappert, P.L. Pye, G.M. McLaughlin, J. Chem. Soc. Dalton Trans. (1984) 1307. (d) M.F. Lappert, P.L. Pye, J. Chem. Soc. Dalton Trans. (1977) 1283.
    • (1984) J. Chem. Soc. Dalton Trans. , pp. 1307
    • Lappert, M.F.1    Pye, P.L.2    McLaughlin, G.M.3
  • 30
    • 37049105203 scopus 로고
    • (d)
    • Detailed IR studies of analogous carbene complexes can be found in (a) K. Öfele, M. Herberhold, Z. Naturforsch. 28 (1973) 306. (b) P.B. Hitchcock, M.F. Lappert, P.L. Pye, J. Chem. Soc. Dalton Trans. (1977) 2160. (c) M.F. Lappert, P.L. Pye, G.M. McLaughlin, J. Chem. Soc. Dalton Trans. (1984) 1307. (d) M.F. Lappert, P.L. Pye, J. Chem. Soc. Dalton Trans. (1977) 1283.
    • (1977) J. Chem. Soc. Dalton Trans. , pp. 1283
    • Lappert, M.F.1    Pye, P.L.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.