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DOI: 10.1055/s-2005-862380
The Pauson-Khand-Type Reaction Catalyzed by Transition Metal Nanoparticles
Publikationsverlauf
Publikationsdatum:
22. Februar 2005 (online)

Abstract
In this account, we survey our work on the use of transition metal nanoparticles as catalysts in Pauson-Khand-type reactions. Cobalt nanoparticles and Co/Ru, Co/Rh, and Co/Pd heterobimetallic nanoparticles have been used in Pauson-Khand-type reactions and related tandem reactions. In the case of Co/Ru nanoparticles, pyridylmethylformate can be used instead of carbon monoxide. We have developed environmentally friendly processes. The use of Co/Rh heterobimetallic nanoparticles allows the development of a new type of [2+2+1] cycloaddition of an α,β-unsaturated aldehyde with an alkyne.
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1 Introduction
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2 Cobalt on Mesoporous Silica: The First Heterogeneous PKR Catalyst
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3 Colloidal Cobalt Nanoparticles
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3.1 The First Use of Transition Metal Nanoparticles in the PKR
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3.2 The First Catalytic PKR in Aqueous Media: Water-Stabilized Colloidal Cobalt Nanoparticles
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4 Immobilized Cobalt Nanoparticles on Charcoal
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4.1 Pauson-Khand Reaction
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4.2 The Catalytic Reductive Pauson-Khand Reaction
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5 Heterobimetallic Nanoparticles
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5.1 Ru/Co Heterobimetallic Nanoparticles: Catalytic Pauson-Khand Reactions in the Presence of Pyridylmethylformate
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5.2 Rh/Co Heterobimetallic Nanoparticles: Catalytic Pauson-Khand-Type Reaction between Alkynes and Olefinic Aldehydes
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5.3 Palladium and Cobalt Nanoparticles Immobilized on Silica: One-Pot Synthesis of Bicyclic Enones by Catalytic Allylic Alkylation and Pauson-Khand Reaction
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6 Use of a Combination of Cobalt Nanoparticles and Pd(II) Complex as a Catalyst in the Synthesis of Fenestranes
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7 Conclusion
Key words
Pauson-Khand reaction - cobalt - heterobimetallic - nanoparticles - heterogeneous catalysis
- 1a
Nakamura I.Yamamoto Y. Chem. Rev. 2004, 104: 2127 - 1b
Zeni G.Larock RC. Chem. Rev. 2004, 104: 2285 - 1c
Hartwig JF. In Comprehensive Coordination Chemistry II Vol. 9:McCleverty JA.Meyer TJ. Elsevier; Oxford UK: 2004. p.369-398 - 1d
Fairlamb IJS. Ann. Rep. Prog. Chem., Sect. B: Org. Chem. 2003, 99: 104 - 1e
Li C.-L.Liu RS. Chem. Rev. 2000, 100: 3127 - 1f
Zimmer R.Dinesh CU.Nandanan E.Khand FA. Chem. Rev. 2000, 100: 3067 - 1g
Beletskaya IP.Cheprakov AV. Chem. Rev. 2000, 100: 3009 - 1h
Yet L. Chem. Rev. 2000, 100: 2963 - 1i
Saito S.Yamamoto Y. Chem. Rev. 2000, 100: 2901 - 1j
Tsuji J. Transition Metal Reagents and Catalysis Wiley and Sons; Susex UK: 2000. - 1k
Transition Metals for Organic Syntheses
Beller M.Bolm C. Wiley-VCH; Weinheim, Germany: 1998. - For selected recent reviews see:
- 2a
Alcaide B.Almendros P. Eur. J. Org. Chem. 2004, 3377 - 2b
Blanco-Urgoiti J.A L.orbe Pérez-Serrano L.Dominguez G.Pérez-Castells J. Chem. Soc. Rev. 2004, 33: 32 - 2c
Gibson SE.Stevenazzi A. Angew. Chem. Int. Ed. 2003, 42: 1800 - 2d
Hanson BE. Comments Inorg. Chem. 2002, 23: 289 - 2e
Brummond KM.Kent JL. Tetrahedron 2000, 56: 3263 - 2f
Fletcher AJ.Christie SDR. J. Chem. Soc., Perkin Trans. 1 2000, 1657 - 2g
Chung YK. Coord. Chem. Rev. 1999, 188: 297 - 2h
Geis O.Schmalz H.-G. Angew. Chem. Int. Ed. 1998, 37: 911 - 3a
Khand IU.Knox GR.Pauson PL.Watts WE. J. Chem. Soc., Chem. Commun. 1971, 36 - 3b
Khand IU.Knox GR.Pauson PL.Watts WE.Foreman MI. J. Chem. Soc., Perkin Trans. 1 1973, 977 - 4a
Krafft ME.Wright JA.Bonaga LVR. Tetrahedron Lett. 2003, 44: 3417 - 4b
Blanco-Urgoiti J.Casarrubios L.Dominguez G.Perez-Castells J. Tetrahedron Lett. 2002, 43: 5763 - 4c
Iqbal M.Vyse N.Dauvergne J.Evans P. Tetrahedron Lett. 2002, 43: 7859 - 4d
Ford JG.Kerr WJ.Kirk GG.Lindsay DM.Middlemiss D. Synlett 2000, 1415 - 4e
Kerr WJ.Lindsay DM.McLaughlin M.Pauson PL. Chem. Commun. 2000, 1467 - 4f
Pagenkopf BL.Belanger DB.O’Mahony DJR.Livinghouse T. Synthesis 2000, 1009 - 4g
Pagenkopf BL.Livinghouse T. J. Am. Chem. Soc. 1996, 118: 2285 - 4h
Smit VA.Simonyan SO.Tarasov VA.Mikaelyan GS.Gybin AS.Ibragimov II.Caple R.Froen D.Kreager A. Synthesis 1989, 472 - 5a
Shambayati S.Crowe WE.Schreiber SL. Tetrahedron Lett. 1990, 31: 5289 - 5b
Jeong N.Chung YK.Lee BY.Lee SH.Yoo S.-E. Synlett 1991, 204 - 5c
Lee BY.Moon H.Chung YK.Jeong N.Pauson PL.Hudecek M. Organometallics 1993, 12: 220 - 5d
Stumpf A.Jeong N.Hwang S. Synlett 1997, 205 - 5e
Derdau V.Laschat S. J. Organomet. Chem. 2002, 642: 131 - 5f
Sugihara T.Yamada M.Yamaguchi M.Nishizawa M. Synlett 1999, 771 - 6a
Kerr WJ.Lindsay DM.Watson SP. Chem. Commun. 1999, 2551 - 6b
Brown DS.Campbell E.Kerr WJ.Lindsay DM.Morrison AJ.Pike KG.Watson SP. Synlett 2000, 1573 - 7a
Lee BY.Chung YK.Hwang Lee Y.Jeong N. J. Am. Chem. Soc. 1994, 116: 8793 - 7b
Kim JW.Chung YK. Synthesis 1998, 142 - 8
Lee NY.Chung YK. Tetrahedron Lett. 1996, 37: 3145 - 9a
Johnson BFG. Coord. Chem. Rev. 1999, 190 - 9b
Corain B.Králik M. J. Mol. Catal. A: Chem. 2001, 173: 99 - 9c
Králik M.Bifffis A. J. Mol. Catal. A: Chem. 2001, 177: 113 - 9d
Astruc D.Chardac F. Chem. Rev. 2001, 101: 2991 - 9e
Thomas JM.Raja R. Chem. Rec. 2001, 1: 448 - 9f
Roucoux A.Schulz J.Patin H. Chem. Rev. 2002, 102: 3757 - 9g
Gai PL.Roper R.White MG. Curr. Opin. Solid State Mater. Sci. 2002, 6: 401 - 9h
Moreno-Manas M.Pleixats R. Acc. Chem. Res. 2003, 36: 638 - 9i
Bell AT. Science 2003, 299: 1688 - 9j
Schlogl R.Abd Hamid SB. Angew. Chem. Int. Ed. 2004, 43: 1628 - 10a
Goia DY.Matijevi E. New J. Chem. 1998, 1203 - 10b
Toshima N.Yonezawa T. New J. Chem. 1998, 1179 - 10c
Ramachandra CN.Kulkarni GU.Thomas PJ.Edwards PP. Chem. Soc. Rev. 2000, 29: 27 - 10d
Corriu RJP. Eur. J. Inorg. Chem. 2001, 1109 - 10e
Rao CNR.Cheetham AK. J. Mater. Chem. 2001, 11: 2887 - 10f
Bönnemann H.Richards RM. Eur. J. Inorg. Chem. 2001, 2455 - 10g
Caruso F. Adv. Mater. 2001, 13: 11 - 10h Rao C. N. R., Kulkarni G. U., Thomas P. J., Edwards P. P.; Chem.-Eur. J.; 2002, 8: 29
- 11a
Kim S.-W.Son SU.Lee S.-I.Hyeon T.Chung YK. J. Am. Chem. Soc. 2000, 122: 1550 - 11b
Son SU.Lee S.-I.Chung YK. Angew. Chem. Int. Ed. 2000, 39: 4158 - 12a
Comley AC.Gibson SE.Hales NJ. Chem. Commun. 2000, 305 - 12b
Dahan A.Portnoy M. Chem. Commun. 2002, 2700 - 13a
Corma A. Chem. Rev. 1997, 97: 2373 - 13b
Mesoporous Molecular Sieves
Bonneviot L.Béland F.Danumah C.Giasson S.Kaliaguine S. Elsevier; Amsterdam: 1998. - 14a
Blanco-Urgoiti J.Casarrubios L.Dominguez G.Perez-Castells J. Tetrahedron Lett. 2002, 43: 5763 - 14b
Sugihara T.Yamaguchi M. Synlett 1998, 1384 - 15
Kim S.-W.Son SU.Chung YK.Hyeon T. Chem. Commun. 2001, 2212 - 16a
Johnson BFG. Topics Catal. 2003, 24: 147 - 16b
Aikin JD.Finke RG. J. Mol. Catal. A: Chem. 1999, 145: 1 - 17a
Beller M.Fischer H.Kuhlein K.Reisinger C.-P.Hermann WA. J. Organomet. Chem. 1996, 520: 257 - 17b
Reetz MT.Lohmer G. Chem. Commun. 1996, 1921 - 17c
Reetz MT.Westermann E. Angew. Chem. Int. Ed. 2000, 39: 165 - 18a
Suslick KS.Fang M.Hyeon T. J. Am. Chem. Soc. 1996, 118: 11960 - 18b
Puntes VF.Krishman KM.Alivisatos AP. Science 2001, 291: 2115 - 18c
Sun S.Murray CB. J. Appl. Phys. 1999, 85: 4325 - 18d
Russier V.Petit C.Legrand J.Pileni MP. Phys. Rev. B. 2000, 62: 3910 - 19
Son SU.Lee SI.Chung YK.Kim S.-W.Hyeon T. Org. Lett. 2002, 4: 277 - 20a
Jeong N.Hwang SH.Lee YW.Lim JS. J. Am. Chem. Soc. 1997, 119: 10549 - 20b
Jeong N.Hwang SH. Angew. Chem. Int. Ed. 2000, 39: 636 - 21a
Ershov BG.Ssukhov NL.Janata E. J. Phys. Chem. B 2000, 104: 6138 - 21b
Russier V.Petit C.Legrand J.Pileni MP. Phys. Rev. B 2000, 62: 3910 - 22
Son SU.Park KH.Chung YK. Org. Lett. 2002, 4: 3983 - 23
Handbook of Coordination, In Catalysis in Organic Chemistry
Chaloner PA. Butterworth; London: 1986. p.38 - 24
Park KH.Son SU.Chung YK. Chem. Commun. 2003, 1898 - 25a
Buchan C.Hamel N.Woell JB.Alper H. J. Chem. Soc., Chem. Commun. 1986, 167 - 25b
Castanet Y.Mortreux A.Petit F. J. Mol. Catal. 1990, 63: 313 - 25c
Carpentier JF.Castanet Y.Brocard J.Mortreux A.Petit F. Tetrahedron Lett. 1991, 32: 4705 - 26a
Simmonata J.-P.Walter T.Métivier P. J. Mol. Catal. A 2001, 171: 91 - 26b
Ko S.Lee C.Choi M.-G.Na Y.Chang S. J. Org. Chem. 2003, 68: 1607 - 26c
Fuji K.Morimoto T.Tsutsumi K.Kakiuchi K. Angew. Chem. Int. Ed. 2003, 42: 2409 - 26d
Morimoto M.Kakiuchi K. Angew. Chem. Int. Ed. 2004, 43: 5580 - 26e
Shibata T.Toshida N.Kogai K. J. Org. Chem. 2002, 67: 7446 - 26f
Shibata T.Toshida N.Kogai K. Org. Lett. 2002, 4: 1619 - 26g
Morimoto T.Fuji K.Tsutsumi K.Kakiuchi K. J. Am. Chem. Soc. 2002, 124: 3806 - 27a
Orince RH.Raspin KA. J. Chem. Soc. A 1969, 612 - 27b
Smolik J.Kraus M. Coll. Czech. Chem. Commun. 1972, 37: 3042 - 28a
Chatani N.Tatamidani H.Ie Y.Kakiuchi F.Murai S. J. Am. Chem. Soc. 2001, 123: 4849 - 28b
Coalter JN.Huffman JC.Caulton KG. Organometallics 2000, 19: 3569 - 28c
Hiraki K.Kira S.Kawano H. Bull. Chem. Soc. Jpn. 1997, 70: 1583 - 29
Park KH.Jung IG.Chung YK. Org. Lett. 2004, 6: 1183 - 30a
Sinfelt JH. Bimetallic Catalysts: Discoveries Concepts and Applications Exxon Monograph, Wiley; New York: 1983. - 30b
Scott RW.Datye AK.Crooks RM. J. Am. Chem. Soc. 2003, 125: 3708 - 30c
Chung YM.Rhee HK. Catal. Lett. 2003, 85: 159 - 30d
David RJ.Boudert M. J. Phys. Chem. 1994, 98: 5471 - 31a
Koga Y.Kobayashi T.Narasaka K. Chem. Lett. 1998, 249 - 31b
Jeong N.Lee S.Sung BK. Organometallics 1998, 17: 3642 - 31c
Kobayashi T.Koga Y.Narasaka K. J. Organomet. Chem. 2001, 624: 73 - 31d
Jeong N.Sung BK.Choi YK. J. Am. Chem. Soc. 2001, 123: 4609 - 31e
Mukai C.Nomura I.Yamanishi K.Hanaoka M. Org. Lett. 2002, 4: 1755 - 31f
Shibata T.Takagi K. J. Am. Chem. Soc. 2000, 122: 9852 - 32a
Thomas JM.Johnson BFG.Raja R.Sankar G.Midgley PA. Acc. Chem. Res. 2003, 36: 20 ; and references therein - 32b
Raja R.Khimyak T.Thomas JM.Hermans S.Johnson BFG. Angew. Chem. Int. Ed. 2001, 40: 4638 - 32c
Hermnas S.Raja R.Thomas JM.Johnson BFG. Angew. Chem. Int. Ed. 2001, 40: 1211 - 32d
Shephard DS.Maschmeyer T.Sankar G.Thomas JM.Ozkaya D.Johnson BFG.Raja R.Oldroyd RD.Bell RG. Chem.-Eur. J. 1998, 4: 1214 - 32e
Nashner MS.Frenkel AI.Adler DL.Shapley JR.Nuzzo RG. J. Am. Chem. Soc. 1997, 119: 7760 - 32f
Nashner MS.Frenkel AI.Somerville D.Hills CW.Shapley JR.Nuzzo RG. J. Am. Chem. Soc. 1998, 120: 8093 - 32g
Hills CW.Nashner MS.Frenkel AI.Shapley JR.Nuzzo RG. Langmuir 1999, 15: 690 - 33a
Thomas JM. Angew. Chem. Int. Ed. 1999, 38: 3588 - 33b
Zou W.Thomas JM.Shephard DS.Johnson BFG.Ozkaya D.Maschmeyer T.Bell RG.Ge Q. Science 1998, 280: 705 - 33c
Nanoscale Materials in Chemistry
Klabunde KJ. John Wiley and Sons Inc.; New York: 2001. p.7 - 34a
Bohm D.Hamann J.Kripylo P. J. Prak. Chem. 1990, 332: 710 - 34b
Brown NF.Barteau MA. J. Am. Chem. Soc. 1992, 114: 4258 - 34c
Rupp R.Huttner G.Rutsch P.Winterhalter U.Barth A.Kricher P.Zsolnai L. Eur. J. Inorg. Chem. 2000, 523 - 35a
Khand IU.Mahaffy CAL.Pauson PL. J. Chem. Res., Miniprint 1978, 4454 - 35b
Krafft ME.Romero RH.Scott IL. J. Org. Chem. 1992, 57: 5277 - 36a
Ahmar M.Antras F.Cazes B. Tetrahedron Lett. 1999, 40: 5503 - 36b
Rivero MR.Adrio J.Carretero C. Eur. J. Org. Chem. 2002, 2881 - 36c
Rivero MR.Carretero C. J. Org. Chem. 2003, 68: 2975 - 37
Khand IU.Pauson PL. J. Chem. Res., Synop. 1977, 9 - 38
Park KH.Son SU.Chung YK. Org. Lett. 2002, 4: 4361 - 39a
Bamhart RW.Barzan GC. J. Am. Chem. Soc. 1998, 120: 1082 - 39b
Evans PA.Robinson JE. J. Am. Chem. Soc. 2001, 123: 4609 - 40a
Coloma F.Liorca J.Homs N.de la Piscina PR.Rodriguez-Reinoso F.Sepulveda-Escribano A. Phys. Chem. Chem. Phys. 2000, 3063 - 40b
Hermans S.Raja R.Thomas JM.Johnson BFG.Sankar G.Gleeson D. Angew. Chem. Int. Ed. 2001, 40: 1211 - 40c
Shephard DS.Maschmeyer T.Sankar G.Thomas JM.Ozkaya D.Johnson BFG.Raja R.Oldroyd RD.Bell RG. Chem.-Eur. J. 1998, 4: 1214 - 41
Jeong N.Seo S.-D.Shin JY. J. Am. Chem. Soc. 2000, 122: 10220 - 42
Son SU.Park KH.Chung YK. J. Am. Chem. Soc. 2002, 124: 6838 - 43a
Thommen M.Veretenov A.Guidetti-Grept R.Keese R. Helv. Chim. Acta 1996, 79: 461 - 43b
Kuck D. In Advances in Theoretically Interesting Molecules Vol. 4:Thummel RP. JAI Press; Greenwich, CT: 1998. p.81 - 44
Kim DH.Son SU.Chung YK.Lee S.-G. Chem. Commun. 2002, 56