Zobrazeno 1 - 10 of 18 pro vyhledávání: '"Tom Nijbacker"'
1
Jet Fuel Synthesis from Syngas Using Bifunctional Cobalt-Based Catalysts
Autor: Evert Boymans, Tom Nijbacker, Dennis Slort, Sander Grootjes, Berend Vreugdenhil
Publikováno v: Catalysts; Volume 12; Issue 3; Pages: 288
Advanced biofuels are required to facilitate the energy transition away from fossil fuels and lower the accompanied CO2 emissions. Particularly, jet fuel needs a renewable substitute, for which novel production routes and technology are needed that a
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::72d0f7fc03ed8c1ffcd7bb3c59af50e5
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2
Phosphinidene Addition to Conjugated Allenes
Autor: Federica Bertini, C. M. D. Komen, Franciscus J. J. de Kanter, Jan B. M. Wit, Murat Ünal, J. Chris Slootweg, Anthony L. Spek, Koop Lammertsma, Andreas W. Ehlers, Martin Lutz, Tom Nijbacker, Marius Schakel
Publikováno v: Advanced Synthesis and Catalysis, 351(7-8), 1132-1138. Wiley-VCH Verlag
Bertini, F, Wit, J B M, Unal, M, de Kanter, F J J, Schakel, M, Slootweg, J C, Ehlers, A W, Nijbacker, T, Komen, C M D, Lutz, M, Spek, A L & Lammertsma, K 2009, ' Phosphinidene Addition to Conjugated Allenes ', Advanced Synthesis and Catalysis, vol. 351, no. 7-8, pp. 1132-1138 . https://doi.org/10.1002/adsc.200900005
Generating the transient electrophilic tungsten pentacarbonyl-phenylphosphinidene complex PhPW(CO)5 in the presence of 2,7-dimethylocta-2,3,5,6-tetraene leads to the formation of a 3,4-disubstituted phosphole or a complexed phospholene, depending on
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b2071ca3adf34640c4cd68d8b3b3e661
https://hdl.handle.net/1871/31413
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3
Syntheses and reactions of terminal Osmium and Ruthenium complexed phosphinidenes n6-Ar(L)M=PMes*
Autor: Marius Schakel, Martin Lutz, Koop Lammertsma, Tom Nijbacker, Arjan T. Termaten, Anthony L. Spek
Publikováno v: Chemistry: A European Journal, 9, 2200-2208. Wiley-VCH Verlag
Termaten, A T, Nijbacker, T, Schakel, M, Lutz, M, Spek, A L & Lammertsma, K 2003, ' Syntheses and reactions of terminal Osmium and Ruthenium complexed phosphinidenes n6-Ar(L)M=PMes* ', Chemistry: A European Journal, vol. 9, pp. 2200-2208 . https://doi.org/10.1002/chem.200204582
Novel, very stable ruthenium and osmium containing terminal phosphinidene complexes [(eta(6)-Ar)(L)M=Mes*] (Ar=benzene, p-cymene; L=PR(3), CO, and RNC) have been prepared by dehydrohalogenation of novel [(eta(6)-Ar)MX(2)(PH(2)Mes*)] complexes in the
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8da80d59fe1009b00666a4e7d65d03a2
https://hdl.handle.net/1871.1/118a3011-b312-4c8a-a7e7-db0dbcadd769
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4
Investigations on 1-Metallaindanes
Autor: Marcel Schreuder Goedheijt, Tom Nijbacker, Otto S. Akkerman, Franciscus J. J. de Kanter, Andrew D. Horton, Friedrich Bickelhaupt
Publikováno v: Schreuder Goedheijt, M, Nijbacker, T, Horton, A D, De Kanter, F J J, Akkerman, O S & Bickelhaupt, F 2003, ' Investigations on 1-Metallaindanes ', European Journal of Inorganic Chemistry, pp. 638-643 . https://doi.org/10.1002/ejic.200390088
European Journal of Inorganic Chemistry, 638-643. Wiley-VCH Verlag
STARTPAGE=638;ENDPAGE=643;ISSN=1434-1948;TITLE=European Journal of Inorganic Chemistry
1-Mercuraindane (6) was prepared in three steps from 1-bromo-2-(2-bromoethyl)benzene (3) and converted into 1-magnesaindane (1) by reaction with magnesium. In solution, 6 was observed to occur in a remarkable dimer/trimer equilibrium, whereas 1 forms
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf79b21f1765474e0552ffd1d46d7315
https://hdl.handle.net/1871.1/a2f4a60f-e217-4373-b65f-bea3ae9395bd
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5
Oligomeric 1,2-dihydro-1-magnesacyclobuta[a]naphthalene
Autor: Tom Nijbacker, Marcel Schreuder Goedheijt, Otto S. Akkerman, Friedrich Bickelhaupt, Franciscus J. J. de Kanter
Publikováno v: Nijbacker, T, Schreuder Goedheijt, M, De Kanter, F J J, Akkerman, O S & Bickelhaupt, F 2002, ' Oligomeric 1,2-dihydro-1-magnesacyclobuta[a]naphthalene ', Main Group Metal Chemistry, vol. 25, pp. 121-127 . https://doi.org/10.1515/MGMC.2002.25.3.121
Main Group Metal Chemistry, 25, 121-127. Walter de Gruyter GmbH
Main Group Metal Chemistry, Vol 25, Iss 3, Pp 121-128 (2002)
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https://doi.org/10.1515/MGMC.2002.25.3.121
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6
Synthesis of Novel Terminal Iridium Phosphinidene Complexes
Autor: Arjan T. Termaten, Koop Lammertsma, Tom Nijbacker, A. L. Spek, Martin Lutz, Marius Schakel
Publikováno v: Termaten, A T, Nijbacker, T, Schakel, M, Lutz, M, Spek, A L & Lammertsma, K 2002, ' Synthesis of Novel Terminal Iridium Phosphinidene Complexes ', Organometallics, vol. 21, pp. 3196-3202 . https://doi.org/10.1021/om020062t
Organometallics, 21, 3196-3202. American Chemical Society
Stable, crystalline iridium-complexed phosphinidenes, Cp*(L)IrPR, are readily synthesized by (a) the reaction of Cp*(L)IrCl2 (2, L = PPh3) with LiPHMes* and (b) dehydrohalogenation of Cp*(PH2R)IrCl2 (5, R = Mes*, Is, Mes) with in situ capturing of tr
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d16929b7f3041f612285ee194528d7b8
https://doi.org/10.1021/om020062t
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7
The 2-Vinylphosphirane-3-Phospholene Rearrangement: Biradicaloid and Concerted Features
Autor: M. J. Van Eis, F. J. J. De Kanter, Tom Nijbacker, F.M. Bickelhaupt, W. H. De Wolf, Koop Lammertsma
Publikováno v: Journal of the American Chemical Society, 122, 3033-3036. American Chemical Society
Van Eis, M J, Nijbacker, T, De Kanter, F J J, De Wolf, W H, Lammertsma, K & Bickelhaupt, F 2000, ' The 2-Vinylphosphirane-3-Phospholene Rearrangement: Biradicaloid and Concerted Features ', Journal of the American Chemical Society, vol. 122, pp. 3033-3036 . https://doi.org/10.1021/ja993829q
Activation parameters have been determined for the 2-vinylphosphirane-3- phospholene rearrangement in the cycloheptane annellated series 7 → 8. For the thermal reaction, the mean activation parameters (ΔH(+) = 125 ± 5 kJ mol
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a73f0ca8f26b991e3ed47e3ff8925f19
https://hdl.handle.net/1871/25300
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10
Generating and dimerizing the transient 16-electron phosphinidene complex [Cp*Ir=PAr]: a theoretical and experimental study
Autor: Anthony L. Spek, Koop Lammertsma, Tom Nijbacker, Andreas W. Ehlers, Arjan T. Termaten, Marius Schakel, Martin Lutz, Michael L. McKee
Publikováno v: Termaten, A T, Nijbacker, T, Ehlers, A W, Schakel, M, Lutz, M, Spek, A L, McKee, M & Lammertsma, K 2004, ' Generating and dimerizing the transient 16-electron phosphinidene complex [Cp*Ir=PAr]: a theoretical and experimental study ', Chemistry: A European Journal, vol. 10, no. 16, pp. 4063-4072 . https://doi.org/10.1002/chem.200400080
Chemistry: A European Journal, 10(16), 4063-4072. Wiley-VCH Verlag
The properties of the 16-electron phosphinidene complex [CpRIr=PR] were investigated experimentally and theoretically. Density functional theory calculations show a preferred bent geometry for the model complex [CpIr=PH], in contrast to the linear st
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3e3e494d517f8519c57c170ac6bae421
https://pubmed.ncbi.nlm.nih.gov/15316986
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