메뉴 건너뛰기




Volumn 35, Issue 2, 1996, Pages 514-525

Synthesis of Polysiloxane-Bound (Ether-phosphine)palladium Complexes. Stoichiometric and Catalytic Reactions in Interphases 1

Author keywords

[No Author keywords available]

Indexed keywords


EID: 0000190245     PISSN: 00201669     EISSN: None     Source Type: Journal    
DOI: 10.1021/ic950412m     Document Type: Article
Times cited : (34)

References (104)
  • 12
    • 0004168292 scopus 로고
    • Brinker, C. J., Clark, D. E., Ulrich, D. R., Eds.; Elsevier: New York
    • Rice, R. In Better Ceramics Through Chemistry; Brinker, C. J., Clark, D. E., Ulrich, D. R., Eds.; Elsevier: New York, 1984.
    • (1984) Better Ceramics Through Chemistry
    • Rice, R.1
  • 21
    • 0003348688 scopus 로고
    • Fricke, J., Ed ; Springer-Verlag: New York
    • (c) Schuck, G.; Dietrich, W.; Fricke, J. In Aerogels; Fricke, J., Ed ; Springer-Verlag: New York, 1986.
    • (1986) Aerogels
    • Schuck, G.1    Dietrich, W.2    Fricke, J.3
  • 46
    • 0001387270 scopus 로고
    • John Wiley & Sons: New York, Collective
    • Conrad, C. R.; Dolliver, M. A. Organic Syntheses; John Wiley & Sons: New York, 1943; Collective Vol. 2, p 167.
    • (1943) Organic Syntheses , vol.2 , pp. 167
    • Conrad, C.R.1    Dolliver, M.A.2
  • 51
    • 2742591018 scopus 로고    scopus 로고
    • The given formula is the repeating unit of a polymer
    • The given formula is the repeating unit of a polymer.
  • 52
    • 2742581180 scopus 로고    scopus 로고
    • note
    • The numbers of the compounds (1-7) represents the stereochemistry of the complexes and the ligands, respectively. The letters a, b designate the type of the ligand. The silicon units involved in the complex are outlined by the letters T and Q. Their stoichiometric amounts are described by a subscript. The letters n and m or the numbers 0-4 define whether the compound is polycondensed (n, m or 1-4) or not (0); see Table 1.
  • 59
    • 2742614394 scopus 로고    scopus 로고
    • note
    • Only a few trans-phosphine palladium complexes exhibit small P-P coupling constants.
  • 77
    • 2742591015 scopus 로고    scopus 로고
    • Eur. Pat. Appl. 376, 364, 1989
    • Spiroketals are supposed to be converted thermally to the analogous polyketones at the applied temperatures. Van Doom, J. A.; Wong, P. K.; Sudmeier, O. Eur. Pat. Appl. 376, 364, 1989: Chem. Abstr. 1991, 114, 24797.
    • Van Doom, J.A.1    Wong, P.K.2    Sudmeier, O.3
  • 78
    • 9144223502 scopus 로고
    • Spiroketals are supposed to be converted thermally to the analogous polyketones at the applied temperatures. Van Doom, J. A.; Wong, P. K.; Sudmeier, O. Eur. Pat. Appl. 376, 364, 1989: Chem. Abstr. 1991, 114, 24797.
    • (1991) Chem. Abstr. , vol.114 , pp. 24797
  • 79
    • 85086527950 scopus 로고    scopus 로고
    • note
    • 13C signal.
  • 80
    • 2742562510 scopus 로고    scopus 로고
    • note
    • 1H} NMR spectra.
  • 81
    • 2742521889 scopus 로고    scopus 로고
    • With x = 1, 2, 3, 4, 5. and 6 the obtained chain lenghts are n = 2, 100, 180, 45, 6, and 2, respectively (see ref 60).
    • With x = 1, 2, 3, 4, 5. and 6 the obtained chain lenghts are n = 2, 100, 180, 45, 6, and 2, respectively (see ref 60).
  • 89
    • 0000702671 scopus 로고
    • For recent publications concerning the Heck reaction see also the following: (a) Heck, R. F. Org. React. 1982, 27, 345 (b) Heck, R. F. Palladium Reagents in Organic Synthesis; Academic Press: New York, 1985. (c) De Meijere, A.; Meyer, F. E. Angew. Chem., Int. Ed. Engl. 1994, 33, 2379 and references cited therein, (d) Cabri, W.; Candiani, I. Acc. Chem. Res. 1995, 28, 2. (e) Cabri, W.; Candiani, I.; de Bernardini, S., Francalanci, F., Penco, S. J. Org. Chem. 1991, 56, 5796. (f) Portmoy, M.; Ben-David, Y.; Rousso, I.; Milstein, D. Organometallics 1994, 13, 3465. (g) Ben-David, J. Portmoy, M.; Gozin, M.; Milstein, D. Organometallics 1992, 11, 1995. (h) Tietze, L. F.; Beifuss, U. Angew. Chem., Int. Ed. Engl. 1993, 32, 131.
    • (1982) Org. React. , vol.27 , pp. 345
    • Heck, R.F.1
  • 90
    • 0003624033 scopus 로고
    • Academic Press: New York
    • For recent publications concerning the Heck reaction see also the following: (a) Heck, R. F. Org. React. 1982, 27, 345 (b) Heck, R. F. Palladium Reagents in Organic Synthesis; Academic Press: New York, 1985. (c) De Meijere, A.; Meyer, F. E. Angew. Chem., Int. Ed. Engl. 1994, 33, 2379 and references cited therein, (d) Cabri, W.; Candiani, I. Acc. Chem. Res. 1995, 28, 2. (e) Cabri, W.; Candiani, I.; de Bernardini, S., Francalanci, F., Penco, S. J. Org. Chem. 1991, 56, 5796. (f) Portmoy, M.; Ben-David, Y.; Rousso, I.; Milstein, D. Organometallics 1994, 13, 3465. (g) Ben-David, J. Portmoy, M.; Gozin, M.; Milstein, D. Organometallics 1992, 11, 1995. (h) Tietze, L. F.; Beifuss, U. Angew. Chem., Int. Ed. Engl. 1993, 32, 131.
    • (1985) Palladium Reagents in Organic Synthesis
    • Heck, R.F.1
  • 91
    • 33748647785 scopus 로고
    • and references cited therein
    • For recent publications concerning the Heck reaction see also the following: (a) Heck, R. F. Org. React. 1982, 27, 345 (b) Heck, R. F. Palladium Reagents in Organic Synthesis; Academic Press: New York, 1985. (c) De Meijere, A.; Meyer, F. E. Angew. Chem., Int. Ed. Engl. 1994, 33, 2379 and references cited therein, (d) Cabri, W.; Candiani, I. Acc. Chem. Res. 1995, 28, 2. (e) Cabri, W.; Candiani, I.; de Bernardini, S., Francalanci, F., Penco, S. J. Org. Chem. 1991, 56, 5796. (f) Portmoy, M.; Ben-David, Y.; Rousso, I.; Milstein, D. Organometallics 1994, 13, 3465. (g) Ben-David, J. Portmoy, M.; Gozin, M.; Milstein, D. Organometallics 1992, 11, 1995. (h) Tietze, L. F.; Beifuss, U. Angew. Chem., Int. Ed. Engl. 1993, 32, 131.
    • (1994) Angew. Chem., Int. Ed. Engl. , vol.33 , pp. 2379
    • De Meijere, A.1    Meyer, F.E.2
  • 92
    • 0038584673 scopus 로고
    • For recent publications concerning the Heck reaction see also the following: (a) Heck, R. F. Org. React. 1982, 27, 345 (b) Heck, R. F. Palladium Reagents in Organic Synthesis; Academic Press: New York, 1985. (c) De Meijere, A.; Meyer, F. E. Angew. Chem., Int. Ed. Engl. 1994, 33, 2379 and references cited therein, (d) Cabri, W.; Candiani, I. Acc. Chem. Res. 1995, 28, 2. (e) Cabri, W.; Candiani, I.; de Bernardini, S., Francalanci, F., Penco, S. J. Org. Chem. 1991, 56, 5796. (f) Portmoy, M.; Ben-David, Y.; Rousso, I.; Milstein, D. Organometallics 1994, 13, 3465. (g) Ben-David, J. Portmoy, M.; Gozin, M.; Milstein, D. Organometallics 1992, 11, 1995. (h) Tietze, L. F.; Beifuss, U. Angew. Chem., Int. Ed. Engl. 1993, 32, 131.
    • (1995) Acc. Chem. Res. , vol.28 , pp. 2
    • Cabri, W.1    Candiani, I.2
  • 93
    • 0025999148 scopus 로고
    • For recent publications concerning the Heck reaction see also the following: (a) Heck, R. F. Org. React. 1982, 27, 345 (b) Heck, R. F. Palladium Reagents in Organic Synthesis; Academic Press: New York, 1985. (c) De Meijere, A.; Meyer, F. E. Angew. Chem., Int. Ed. Engl. 1994, 33, 2379 and references cited therein, (d) Cabri, W.; Candiani, I. Acc. Chem. Res. 1995, 28, 2. (e) Cabri, W.; Candiani, I.; de Bernardini, S., Francalanci, F., Penco, S. J. Org. Chem. 1991, 56, 5796. (f) Portmoy, M.; Ben-David, Y.; Rousso, I.; Milstein, D. Organometallics 1994, 13, 3465. (g) Ben-David, J. Portmoy, M.; Gozin, M.; Milstein, D. Organometallics 1992, 11, 1995. (h) Tietze, L. F.; Beifuss, U. Angew. Chem., Int. Ed. Engl. 1993, 32, 131.
    • (1991) J. Org. Chem. , vol.56 , pp. 5796
    • Cabri, W.1    Candiani, I.2    De Bernardini, S.3    Francalanci, F.4    Penco, S.5
  • 94
    • 0000051004 scopus 로고
    • For recent publications concerning the Heck reaction see also the following: (a) Heck, R. F. Org. React. 1982, 27, 345 (b) Heck, R. F. Palladium Reagents in Organic Synthesis; Academic Press: New York, 1985. (c) De Meijere, A.; Meyer, F. E. Angew. Chem., Int. Ed. Engl. 1994, 33, 2379 and references cited therein, (d) Cabri, W.; Candiani, I. Acc. Chem. Res. 1995, 28, 2. (e) Cabri, W.; Candiani, I.; de Bernardini, S., Francalanci, F., Penco, S. J. Org. Chem. 1991, 56, 5796. (f) Portmoy, M.; Ben-David, Y.; Rousso, I.; Milstein, D. Organometallics 1994, 13, 3465. (g) Ben-David, J. Portmoy, M.; Gozin, M.; Milstein, D. Organometallics 1992, 11, 1995. (h) Tietze, L. F.; Beifuss, U. Angew. Chem., Int. Ed. Engl. 1993, 32, 131.
    • (1994) Organometallics , vol.13 , pp. 3465
    • Portmoy, M.1    Ben-David, Y.2    Rousso, I.3    Milstein, D.4
  • 95
    • 0001104162 scopus 로고
    • For recent publications concerning the Heck reaction see also the following: (a) Heck, R. F. Org. React. 1982, 27, 345 (b) Heck, R. F. Palladium Reagents in Organic Synthesis; Academic Press: New York, 1985. (c) De Meijere, A.; Meyer, F. E. Angew. Chem., Int. Ed. Engl. 1994, 33, 2379 and references cited therein, (d) Cabri, W.; Candiani, I. Acc. Chem. Res. 1995, 28, 2. (e) Cabri, W.; Candiani, I.; de Bernardini, S., Francalanci, F., Penco, S. J. Org. Chem. 1991, 56, 5796. (f) Portmoy, M.; Ben-David, Y.; Rousso, I.; Milstein, D. Organometallics 1994, 13, 3465. (g) Ben-David, J. Portmoy, M.; Gozin, M.; Milstein, D. Organometallics 1992, 11, 1995. (h) Tietze, L. F.; Beifuss, U. Angew. Chem., Int. Ed. Engl. 1993, 32, 131.
    • (1992) Organometallics , vol.11 , pp. 1995
    • Ben-David, J.1    Portmoy, M.2    Gozin, M.3    Milstein, D.4
  • 96
    • 33750173220 scopus 로고
    • For recent publications concerning the Heck reaction see also the following: (a) Heck, R. F. Org. React. 1982, 27, 345 (b) Heck, R. F. Palladium Reagents in Organic Synthesis; Academic Press: New York, 1985. (c) De Meijere, A.; Meyer, F. E. Angew. Chem., Int. Ed. Engl. 1994, 33, 2379 and references cited therein, (d) Cabri, W.; Candiani, I. Acc. Chem. Res. 1995, 28, 2. (e) Cabri, W.; Candiani, I.; de Bernardini, S., Francalanci, F., Penco, S. J. Org. Chem. 1991, 56, 5796. (f) Portmoy, M.; Ben-David, Y.; Rousso, I.; Milstein, D. Organometallics 1994, 13, 3465. (g) Ben-David, J. Portmoy, M.; Gozin, M.; Milstein, D. Organometallics 1992, 11, 1995. (h) Tietze, L. F.; Beifuss, U. Angew. Chem., Int. Ed. Engl. 1993, 32, 131.
    • (1993) Angew. Chem., Int. Ed. Engl. , vol.32 , pp. 131
    • Tietze, L.F.1    Beifuss, U.2
  • 97
    • 0000730986 scopus 로고
    • Examples of polymer supported Heck catalysts are reported by the following, (a) Terasawa, M.; Kaneda, K.; Imanaka, T.; Teranishi, S. J. Organomet. Chem. 1978, 162, 403. (b) Anderson, C.-M.; Karabelas, K.; Hallberg, A.; Andersson, C. J. Org. Chem. 1985, 50, 3891. (c) Choudary, B. M.; Sarma, M. R.; Rao, K. K. Tetrahedron Lett. 1990, 31, 5781. (d) Choudary B. M.; Sarma, M. R. Tetrahedron Lett. 1990, 31, 1496. (e) Choudary, B. M.; Sarma, M. R.; Rao, K. K. Tetrahedron 1992, 48, 719.
    • (1978) J. Organomet. Chem. , vol.162 , pp. 403
    • Terasawa, M.1    Kaneda, K.2    Imanaka, T.3    Teranishi, S.4
  • 98
    • 0346541032 scopus 로고
    • Examples of polymer supported Heck catalysts are reported by the following, (a) Terasawa, M.; Kaneda, K.; Imanaka, T.; Teranishi, S. J. Organomet. Chem. 1978, 162, 403. (b) Anderson, C.-M.; Karabelas, K.; Hallberg, A.; Andersson, C. J. Org. Chem. 1985, 50, 3891. (c) Choudary, B. M.; Sarma, M. R.; Rao, K. K. Tetrahedron Lett. 1990, 31, 5781. (d) Choudary B. M.; Sarma, M. R. Tetrahedron Lett. 1990, 31, 1496. (e) Choudary, B. M.; Sarma, M. R.; Rao, K. K. Tetrahedron 1992, 48, 719.
    • (1985) J. Org. Chem. , vol.50 , pp. 3891
    • Anderson, C.-M.1    Karabelas, K.2    Hallberg, A.3    Andersson, C.4
  • 99
    • 0025168554 scopus 로고
    • Examples of polymer supported Heck catalysts are reported by the following, (a) Terasawa, M.; Kaneda, K.; Imanaka, T.; Teranishi, S. J. Organomet. Chem. 1978, 162, 403. (b) Anderson, C.-M.; Karabelas, K.; Hallberg, A.; Andersson, C. J. Org. Chem. 1985, 50, 3891. (c) Choudary, B. M.; Sarma, M. R.; Rao, K. K. Tetrahedron Lett. 1990, 31, 5781. (d) Choudary B. M.; Sarma, M. R. Tetrahedron Lett. 1990, 31, 1496. (e) Choudary, B. M.; Sarma, M. R.; Rao, K. K. Tetrahedron 1992, 48, 719.
    • (1990) Tetrahedron Lett. , vol.31 , pp. 5781
    • Choudary, B.M.1    Sarma, M.R.2    Rao, K.K.3
  • 100
    • 2742536327 scopus 로고
    • Examples of polymer supported Heck catalysts are reported by the following, (a) Terasawa, M.; Kaneda, K.; Imanaka, T.; Teranishi, S. J. Organomet. Chem. 1978, 162, 403. (b) Anderson, C.-M.; Karabelas, K.; Hallberg, A.; Andersson, C. J. Org. Chem. 1985, 50, 3891. (c) Choudary, B. M.; Sarma, M. R.; Rao, K. K. Tetrahedron Lett. 1990, 31, 5781. (d) Choudary B. M.; Sarma, M. R. Tetrahedron Lett. 1990, 31, 1496. (e) Choudary, B. M.; Sarma, M. R.; Rao, K. K. Tetrahedron 1992, 48, 719.
    • (1990) Tetrahedron Lett. , vol.31 , pp. 1496
    • Choudary, B.M.1    Sarma, M.R.2
  • 101
    • 0026540861 scopus 로고
    • Examples of polymer supported Heck catalysts are reported by the following, (a) Terasawa, M.; Kaneda, K.; Imanaka, T.; Teranishi, S. J. Organomet. Chem. 1978, 162, 403. (b) Anderson, C.-M.; Karabelas, K.; Hallberg, A.; Andersson, C. J. Org. Chem. 1985, 50, 3891. (c) Choudary, B. M.; Sarma, M. R.; Rao, K. K. Tetrahedron Lett. 1990, 31, 5781. (d) Choudary B. M.; Sarma, M. R. Tetrahedron Lett. 1990, 31, 1496. (e) Choudary, B. M.; Sarma, M. R.; Rao, K. K. Tetrahedron 1992, 48, 719.
    • (1992) Tetrahedron , vol.48 , pp. 719
    • Choudary, B.M.1    Sarma, M.R.2    Rao, K.K.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.