Synthesis and molecular structures of tris(thio- and selenophenyl)stannyl complexes of cyclopentadienylcarbonylnitrosylmanganese and their reaction products with tungsten carbony
Abstract Reactions of CpMn(CO)(NO)$ SnCl_{3} $ (I) with sodium benzenethiolate and sodium benzenesele-nolate gave orange crystals of the complexes CpMn(CO)(NO)Sn(EPh)3, where E = S (II) or Se (III). Treatment of complex II with photochemically generated W(CO)5(THF) yielded the adduct CpMn(CO)(NO)Sn(...
Ausführliche Beschreibung
Autor*in: |
Pasynskii, A. A. [verfasserIn] Blokhin, A. I. [verfasserIn] Torubaev, Yu. V. [verfasserIn] Dobrokhotova, Zh. V. [verfasserIn] |
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E-Artikel |
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Sprache: |
Englisch |
Erschienen: |
2011 |
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Schlagwörter: |
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Übergeordnetes Werk: |
Enthalten in: Russian journal of coordination chemistry - Moscow : MAIK Nauka/Interperiodica Publ., 2000, 37(2011), 12 vom: Dez., Seite 879-886 |
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Übergeordnetes Werk: |
volume:37 ; year:2011 ; number:12 ; month:12 ; pages:879-886 |
Links: |
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DOI / URN: |
10.1134/S1070328411110108 |
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Katalog-ID: |
SPR017355621 |
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245 | 1 | 0 | |a Synthesis and molecular structures of tris(thio- and selenophenyl)stannyl complexes of cyclopentadienylcarbonylnitrosylmanganese and their reaction products with tungsten carbony |
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520 | |a Abstract Reactions of CpMn(CO)(NO)$ SnCl_{3} $ (I) with sodium benzenethiolate and sodium benzenesele-nolate gave orange crystals of the complexes CpMn(CO)(NO)Sn(EPh)3, where E = S (II) or Se (III). Treatment of complex II with photochemically generated W(CO)5(THF) yielded the adduct CpMn(CO)(NO)Sn(SPh)3 · W(CO)5 (IV). A similar treatment of complex III resulted in the formation of the ditungsten complex $ W_{2} $(CO)4(SePh)6 (V) with transfer of all chalcogenate groups from tin to tungsten. In reactions of complexes II and III with a $ Pt_{0} $ complex with phosphine and acetylene, ($ PPh_{3} $)2Pt($ Ph_{2} %$ C_{2} $), the chalcogenate groups are transferred from tin. Only the known Pt(II) complexes ($ PPh_{3} $)2Pt(EPh)2), where E= S (VI) or Se (VII). Molecular structures IV and V were characterized by X-ray diffraction. It has been found that the Mn-Sn bond in complex IV (2.5479(9) Å) is nearly the same length as that found earlier for complex II (2.5328(17) Å) and is substantially shorter than the sum of the covalent radii of Mn and Sn (2.78 Å). The Sn-S bond is noticeably lengthened (2.5217(11) Å) only for the S atom bound to tungsten (W-S, 2.5696(12) Å), while the other Sn-S bonds (2.4413(12) and 2.4291(12) Å) are virtually the same as in complex II (on average, 2.441 Å). Complex V contains the direct W-W bond (2.8153(16) Å) supplemented with four benzeneselenolate bridges in which the W-Se bonds (on average, 2.642(2) Å) are longer than the two terminal W-SePh bonds (2.571(2) Å). All the W-Se bonds are much shorter than the sum of the covalent radii of W and Se (2.82 Å). | ||
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650 | 4 | |a Pentacarbonyltungsten |7 (dpeaa)DE-He213 | |
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650 | 4 | |a Complex CpMn |7 (dpeaa)DE-He213 | |
700 | 1 | |a Blokhin, A. I. |e verfasserin |4 aut | |
700 | 1 | |a Torubaev, Yu. V. |e verfasserin |4 aut | |
700 | 1 | |a Dobrokhotova, Zh. V. |e verfasserin |4 aut | |
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10.1134/S1070328411110108 doi (DE-627)SPR017355621 (SPR)S1070328411110108-e DE-627 ger DE-627 rakwb eng 540 ASE 35.43 bkl Pasynskii, A. A. verfasserin aut Synthesis and molecular structures of tris(thio- and selenophenyl)stannyl complexes of cyclopentadienylcarbonylnitrosylmanganese and their reaction products with tungsten carbony 2011 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Reactions of CpMn(CO)(NO)$ SnCl_{3} $ (I) with sodium benzenethiolate and sodium benzenesele-nolate gave orange crystals of the complexes CpMn(CO)(NO)Sn(EPh)3, where E = S (II) or Se (III). Treatment of complex II with photochemically generated W(CO)5(THF) yielded the adduct CpMn(CO)(NO)Sn(SPh)3 · W(CO)5 (IV). A similar treatment of complex III resulted in the formation of the ditungsten complex $ W_{2} $(CO)4(SePh)6 (V) with transfer of all chalcogenate groups from tin to tungsten. In reactions of complexes II and III with a $ Pt_{0} $ complex with phosphine and acetylene, ($ PPh_{3} $)2Pt($ Ph_{2} %$ C_{2} $), the chalcogenate groups are transferred from tin. Only the known Pt(II) complexes ($ PPh_{3} $)2Pt(EPh)2), where E= S (VI) or Se (VII). Molecular structures IV and V were characterized by X-ray diffraction. It has been found that the Mn-Sn bond in complex IV (2.5479(9) Å) is nearly the same length as that found earlier for complex II (2.5328(17) Å) and is substantially shorter than the sum of the covalent radii of Mn and Sn (2.78 Å). The Sn-S bond is noticeably lengthened (2.5217(11) Å) only for the S atom bound to tungsten (W-S, 2.5696(12) Å), while the other Sn-S bonds (2.4413(12) and 2.4291(12) Å) are virtually the same as in complex II (on average, 2.441 Å). Complex V contains the direct W-W bond (2.8153(16) Å) supplemented with four benzeneselenolate bridges in which the W-Se bonds (on average, 2.642(2) Å) are longer than the two terminal W-SePh bonds (2.571(2) Å). All the W-Se bonds are much shorter than the sum of the covalent radii of W and Se (2.82 Å). Covalent Radius (dpeaa)DE-He213 Water Aspirator Vacuum (dpeaa)DE-He213 Pentacarbonyltungsten (dpeaa)DE-He213 Selenophenyl (dpeaa)DE-He213 Complex CpMn (dpeaa)DE-He213 Blokhin, A. I. verfasserin aut Torubaev, Yu. V. verfasserin aut Dobrokhotova, Zh. V. verfasserin aut Enthalten in Russian journal of coordination chemistry Moscow : MAIK Nauka/Interperiodica Publ., 2000 37(2011), 12 vom: Dez., Seite 879-886 (DE-627)334712939 (DE-600)2058157-9 1608-3318 nnns volume:37 year:2011 number:12 month:12 pages:879-886 https://dx.doi.org/10.1134/S1070328411110108 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 35.43 ASE AR 37 2011 12 12 879-886 |
spelling |
10.1134/S1070328411110108 doi (DE-627)SPR017355621 (SPR)S1070328411110108-e DE-627 ger DE-627 rakwb eng 540 ASE 35.43 bkl Pasynskii, A. A. verfasserin aut Synthesis and molecular structures of tris(thio- and selenophenyl)stannyl complexes of cyclopentadienylcarbonylnitrosylmanganese and their reaction products with tungsten carbony 2011 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Reactions of CpMn(CO)(NO)$ SnCl_{3} $ (I) with sodium benzenethiolate and sodium benzenesele-nolate gave orange crystals of the complexes CpMn(CO)(NO)Sn(EPh)3, where E = S (II) or Se (III). Treatment of complex II with photochemically generated W(CO)5(THF) yielded the adduct CpMn(CO)(NO)Sn(SPh)3 · W(CO)5 (IV). A similar treatment of complex III resulted in the formation of the ditungsten complex $ W_{2} $(CO)4(SePh)6 (V) with transfer of all chalcogenate groups from tin to tungsten. In reactions of complexes II and III with a $ Pt_{0} $ complex with phosphine and acetylene, ($ PPh_{3} $)2Pt($ Ph_{2} %$ C_{2} $), the chalcogenate groups are transferred from tin. Only the known Pt(II) complexes ($ PPh_{3} $)2Pt(EPh)2), where E= S (VI) or Se (VII). Molecular structures IV and V were characterized by X-ray diffraction. It has been found that the Mn-Sn bond in complex IV (2.5479(9) Å) is nearly the same length as that found earlier for complex II (2.5328(17) Å) and is substantially shorter than the sum of the covalent radii of Mn and Sn (2.78 Å). The Sn-S bond is noticeably lengthened (2.5217(11) Å) only for the S atom bound to tungsten (W-S, 2.5696(12) Å), while the other Sn-S bonds (2.4413(12) and 2.4291(12) Å) are virtually the same as in complex II (on average, 2.441 Å). Complex V contains the direct W-W bond (2.8153(16) Å) supplemented with four benzeneselenolate bridges in which the W-Se bonds (on average, 2.642(2) Å) are longer than the two terminal W-SePh bonds (2.571(2) Å). All the W-Se bonds are much shorter than the sum of the covalent radii of W and Se (2.82 Å). Covalent Radius (dpeaa)DE-He213 Water Aspirator Vacuum (dpeaa)DE-He213 Pentacarbonyltungsten (dpeaa)DE-He213 Selenophenyl (dpeaa)DE-He213 Complex CpMn (dpeaa)DE-He213 Blokhin, A. I. verfasserin aut Torubaev, Yu. V. verfasserin aut Dobrokhotova, Zh. V. verfasserin aut Enthalten in Russian journal of coordination chemistry Moscow : MAIK Nauka/Interperiodica Publ., 2000 37(2011), 12 vom: Dez., Seite 879-886 (DE-627)334712939 (DE-600)2058157-9 1608-3318 nnns volume:37 year:2011 number:12 month:12 pages:879-886 https://dx.doi.org/10.1134/S1070328411110108 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 35.43 ASE AR 37 2011 12 12 879-886 |
allfields_unstemmed |
10.1134/S1070328411110108 doi (DE-627)SPR017355621 (SPR)S1070328411110108-e DE-627 ger DE-627 rakwb eng 540 ASE 35.43 bkl Pasynskii, A. A. verfasserin aut Synthesis and molecular structures of tris(thio- and selenophenyl)stannyl complexes of cyclopentadienylcarbonylnitrosylmanganese and their reaction products with tungsten carbony 2011 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Reactions of CpMn(CO)(NO)$ SnCl_{3} $ (I) with sodium benzenethiolate and sodium benzenesele-nolate gave orange crystals of the complexes CpMn(CO)(NO)Sn(EPh)3, where E = S (II) or Se (III). Treatment of complex II with photochemically generated W(CO)5(THF) yielded the adduct CpMn(CO)(NO)Sn(SPh)3 · W(CO)5 (IV). A similar treatment of complex III resulted in the formation of the ditungsten complex $ W_{2} $(CO)4(SePh)6 (V) with transfer of all chalcogenate groups from tin to tungsten. In reactions of complexes II and III with a $ Pt_{0} $ complex with phosphine and acetylene, ($ PPh_{3} $)2Pt($ Ph_{2} %$ C_{2} $), the chalcogenate groups are transferred from tin. Only the known Pt(II) complexes ($ PPh_{3} $)2Pt(EPh)2), where E= S (VI) or Se (VII). Molecular structures IV and V were characterized by X-ray diffraction. It has been found that the Mn-Sn bond in complex IV (2.5479(9) Å) is nearly the same length as that found earlier for complex II (2.5328(17) Å) and is substantially shorter than the sum of the covalent radii of Mn and Sn (2.78 Å). The Sn-S bond is noticeably lengthened (2.5217(11) Å) only for the S atom bound to tungsten (W-S, 2.5696(12) Å), while the other Sn-S bonds (2.4413(12) and 2.4291(12) Å) are virtually the same as in complex II (on average, 2.441 Å). Complex V contains the direct W-W bond (2.8153(16) Å) supplemented with four benzeneselenolate bridges in which the W-Se bonds (on average, 2.642(2) Å) are longer than the two terminal W-SePh bonds (2.571(2) Å). All the W-Se bonds are much shorter than the sum of the covalent radii of W and Se (2.82 Å). Covalent Radius (dpeaa)DE-He213 Water Aspirator Vacuum (dpeaa)DE-He213 Pentacarbonyltungsten (dpeaa)DE-He213 Selenophenyl (dpeaa)DE-He213 Complex CpMn (dpeaa)DE-He213 Blokhin, A. I. verfasserin aut Torubaev, Yu. V. verfasserin aut Dobrokhotova, Zh. V. verfasserin aut Enthalten in Russian journal of coordination chemistry Moscow : MAIK Nauka/Interperiodica Publ., 2000 37(2011), 12 vom: Dez., Seite 879-886 (DE-627)334712939 (DE-600)2058157-9 1608-3318 nnns volume:37 year:2011 number:12 month:12 pages:879-886 https://dx.doi.org/10.1134/S1070328411110108 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 35.43 ASE AR 37 2011 12 12 879-886 |
allfieldsGer |
10.1134/S1070328411110108 doi (DE-627)SPR017355621 (SPR)S1070328411110108-e DE-627 ger DE-627 rakwb eng 540 ASE 35.43 bkl Pasynskii, A. A. verfasserin aut Synthesis and molecular structures of tris(thio- and selenophenyl)stannyl complexes of cyclopentadienylcarbonylnitrosylmanganese and their reaction products with tungsten carbony 2011 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Reactions of CpMn(CO)(NO)$ SnCl_{3} $ (I) with sodium benzenethiolate and sodium benzenesele-nolate gave orange crystals of the complexes CpMn(CO)(NO)Sn(EPh)3, where E = S (II) or Se (III). Treatment of complex II with photochemically generated W(CO)5(THF) yielded the adduct CpMn(CO)(NO)Sn(SPh)3 · W(CO)5 (IV). A similar treatment of complex III resulted in the formation of the ditungsten complex $ W_{2} $(CO)4(SePh)6 (V) with transfer of all chalcogenate groups from tin to tungsten. In reactions of complexes II and III with a $ Pt_{0} $ complex with phosphine and acetylene, ($ PPh_{3} $)2Pt($ Ph_{2} %$ C_{2} $), the chalcogenate groups are transferred from tin. Only the known Pt(II) complexes ($ PPh_{3} $)2Pt(EPh)2), where E= S (VI) or Se (VII). Molecular structures IV and V were characterized by X-ray diffraction. It has been found that the Mn-Sn bond in complex IV (2.5479(9) Å) is nearly the same length as that found earlier for complex II (2.5328(17) Å) and is substantially shorter than the sum of the covalent radii of Mn and Sn (2.78 Å). The Sn-S bond is noticeably lengthened (2.5217(11) Å) only for the S atom bound to tungsten (W-S, 2.5696(12) Å), while the other Sn-S bonds (2.4413(12) and 2.4291(12) Å) are virtually the same as in complex II (on average, 2.441 Å). Complex V contains the direct W-W bond (2.8153(16) Å) supplemented with four benzeneselenolate bridges in which the W-Se bonds (on average, 2.642(2) Å) are longer than the two terminal W-SePh bonds (2.571(2) Å). All the W-Se bonds are much shorter than the sum of the covalent radii of W and Se (2.82 Å). Covalent Radius (dpeaa)DE-He213 Water Aspirator Vacuum (dpeaa)DE-He213 Pentacarbonyltungsten (dpeaa)DE-He213 Selenophenyl (dpeaa)DE-He213 Complex CpMn (dpeaa)DE-He213 Blokhin, A. I. verfasserin aut Torubaev, Yu. V. verfasserin aut Dobrokhotova, Zh. V. verfasserin aut Enthalten in Russian journal of coordination chemistry Moscow : MAIK Nauka/Interperiodica Publ., 2000 37(2011), 12 vom: Dez., Seite 879-886 (DE-627)334712939 (DE-600)2058157-9 1608-3318 nnns volume:37 year:2011 number:12 month:12 pages:879-886 https://dx.doi.org/10.1134/S1070328411110108 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 35.43 ASE AR 37 2011 12 12 879-886 |
allfieldsSound |
10.1134/S1070328411110108 doi (DE-627)SPR017355621 (SPR)S1070328411110108-e DE-627 ger DE-627 rakwb eng 540 ASE 35.43 bkl Pasynskii, A. A. verfasserin aut Synthesis and molecular structures of tris(thio- and selenophenyl)stannyl complexes of cyclopentadienylcarbonylnitrosylmanganese and their reaction products with tungsten carbony 2011 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Reactions of CpMn(CO)(NO)$ SnCl_{3} $ (I) with sodium benzenethiolate and sodium benzenesele-nolate gave orange crystals of the complexes CpMn(CO)(NO)Sn(EPh)3, where E = S (II) or Se (III). Treatment of complex II with photochemically generated W(CO)5(THF) yielded the adduct CpMn(CO)(NO)Sn(SPh)3 · W(CO)5 (IV). A similar treatment of complex III resulted in the formation of the ditungsten complex $ W_{2} $(CO)4(SePh)6 (V) with transfer of all chalcogenate groups from tin to tungsten. In reactions of complexes II and III with a $ Pt_{0} $ complex with phosphine and acetylene, ($ PPh_{3} $)2Pt($ Ph_{2} %$ C_{2} $), the chalcogenate groups are transferred from tin. Only the known Pt(II) complexes ($ PPh_{3} $)2Pt(EPh)2), where E= S (VI) or Se (VII). Molecular structures IV and V were characterized by X-ray diffraction. It has been found that the Mn-Sn bond in complex IV (2.5479(9) Å) is nearly the same length as that found earlier for complex II (2.5328(17) Å) and is substantially shorter than the sum of the covalent radii of Mn and Sn (2.78 Å). The Sn-S bond is noticeably lengthened (2.5217(11) Å) only for the S atom bound to tungsten (W-S, 2.5696(12) Å), while the other Sn-S bonds (2.4413(12) and 2.4291(12) Å) are virtually the same as in complex II (on average, 2.441 Å). Complex V contains the direct W-W bond (2.8153(16) Å) supplemented with four benzeneselenolate bridges in which the W-Se bonds (on average, 2.642(2) Å) are longer than the two terminal W-SePh bonds (2.571(2) Å). All the W-Se bonds are much shorter than the sum of the covalent radii of W and Se (2.82 Å). Covalent Radius (dpeaa)DE-He213 Water Aspirator Vacuum (dpeaa)DE-He213 Pentacarbonyltungsten (dpeaa)DE-He213 Selenophenyl (dpeaa)DE-He213 Complex CpMn (dpeaa)DE-He213 Blokhin, A. I. verfasserin aut Torubaev, Yu. V. verfasserin aut Dobrokhotova, Zh. V. verfasserin aut Enthalten in Russian journal of coordination chemistry Moscow : MAIK Nauka/Interperiodica Publ., 2000 37(2011), 12 vom: Dez., Seite 879-886 (DE-627)334712939 (DE-600)2058157-9 1608-3318 nnns volume:37 year:2011 number:12 month:12 pages:879-886 https://dx.doi.org/10.1134/S1070328411110108 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 35.43 ASE AR 37 2011 12 12 879-886 |
language |
English |
source |
Enthalten in Russian journal of coordination chemistry 37(2011), 12 vom: Dez., Seite 879-886 volume:37 year:2011 number:12 month:12 pages:879-886 |
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Enthalten in Russian journal of coordination chemistry 37(2011), 12 vom: Dez., Seite 879-886 volume:37 year:2011 number:12 month:12 pages:879-886 |
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Article |
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Covalent Radius Water Aspirator Vacuum Pentacarbonyltungsten Selenophenyl Complex CpMn |
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Russian journal of coordination chemistry |
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Pasynskii, A. A. @@aut@@ Blokhin, A. I. @@aut@@ Torubaev, Yu. V. @@aut@@ Dobrokhotova, Zh. V. @@aut@@ |
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2011-12-01T00:00:00Z |
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A.</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Synthesis and molecular structures of tris(thio- and selenophenyl)stannyl complexes of cyclopentadienylcarbonylnitrosylmanganese and their reaction products with tungsten carbony</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">2011</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">Text</subfield><subfield code="b">txt</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">Computermedien</subfield><subfield code="b">c</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">Online-Ressource</subfield><subfield code="b">cr</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Abstract Reactions of CpMn(CO)(NO)$ SnCl_{3} $ (I) with sodium benzenethiolate and sodium benzenesele-nolate gave orange crystals of the complexes CpMn(CO)(NO)Sn(EPh)3, where E = S (II) or Se (III). Treatment of complex II with photochemically generated W(CO)5(THF) yielded the adduct CpMn(CO)(NO)Sn(SPh)3 · W(CO)5 (IV). A similar treatment of complex III resulted in the formation of the ditungsten complex $ W_{2} $(CO)4(SePh)6 (V) with transfer of all chalcogenate groups from tin to tungsten. In reactions of complexes II and III with a $ Pt_{0} $ complex with phosphine and acetylene, ($ PPh_{3} $)2Pt($ Ph_{2} %$ C_{2} $), the chalcogenate groups are transferred from tin. Only the known Pt(II) complexes ($ PPh_{3} $)2Pt(EPh)2), where E= S (VI) or Se (VII). Molecular structures IV and V were characterized by X-ray diffraction. It has been found that the Mn-Sn bond in complex IV (2.5479(9) Å) is nearly the same length as that found earlier for complex II (2.5328(17) Å) and is substantially shorter than the sum of the covalent radii of Mn and Sn (2.78 Å). The Sn-S bond is noticeably lengthened (2.5217(11) Å) only for the S atom bound to tungsten (W-S, 2.5696(12) Å), while the other Sn-S bonds (2.4413(12) and 2.4291(12) Å) are virtually the same as in complex II (on average, 2.441 Å). Complex V contains the direct W-W bond (2.8153(16) Å) supplemented with four benzeneselenolate bridges in which the W-Se bonds (on average, 2.642(2) Å) are longer than the two terminal W-SePh bonds (2.571(2) Å). 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author |
Pasynskii, A. A. |
spellingShingle |
Pasynskii, A. A. ddc 540 bkl 35.43 misc Covalent Radius misc Water Aspirator Vacuum misc Pentacarbonyltungsten misc Selenophenyl misc Complex CpMn Synthesis and molecular structures of tris(thio- and selenophenyl)stannyl complexes of cyclopentadienylcarbonylnitrosylmanganese and their reaction products with tungsten carbony |
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540 ASE 35.43 bkl Synthesis and molecular structures of tris(thio- and selenophenyl)stannyl complexes of cyclopentadienylcarbonylnitrosylmanganese and their reaction products with tungsten carbony Covalent Radius (dpeaa)DE-He213 Water Aspirator Vacuum (dpeaa)DE-He213 Pentacarbonyltungsten (dpeaa)DE-He213 Selenophenyl (dpeaa)DE-He213 Complex CpMn (dpeaa)DE-He213 |
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ddc 540 bkl 35.43 misc Covalent Radius misc Water Aspirator Vacuum misc Pentacarbonyltungsten misc Selenophenyl misc Complex CpMn |
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ddc 540 bkl 35.43 misc Covalent Radius misc Water Aspirator Vacuum misc Pentacarbonyltungsten misc Selenophenyl misc Complex CpMn |
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Synthesis and molecular structures of tris(thio- and selenophenyl)stannyl complexes of cyclopentadienylcarbonylnitrosylmanganese and their reaction products with tungsten carbony |
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Synthesis and molecular structures of tris(thio- and selenophenyl)stannyl complexes of cyclopentadienylcarbonylnitrosylmanganese and their reaction products with tungsten carbony |
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Pasynskii, A. A. Blokhin, A. I. Torubaev, Yu. V. Dobrokhotova, Zh. V. |
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37 |
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540 ASE 35.43 bkl |
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Elektronische Aufsätze |
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Pasynskii, A. A. |
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10.1134/S1070328411110108 |
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title_sort |
synthesis and molecular structures of tris(thio- and selenophenyl)stannyl complexes of cyclopentadienylcarbonylnitrosylmanganese and their reaction products with tungsten carbony |
title_auth |
Synthesis and molecular structures of tris(thio- and selenophenyl)stannyl complexes of cyclopentadienylcarbonylnitrosylmanganese and their reaction products with tungsten carbony |
abstract |
Abstract Reactions of CpMn(CO)(NO)$ SnCl_{3} $ (I) with sodium benzenethiolate and sodium benzenesele-nolate gave orange crystals of the complexes CpMn(CO)(NO)Sn(EPh)3, where E = S (II) or Se (III). Treatment of complex II with photochemically generated W(CO)5(THF) yielded the adduct CpMn(CO)(NO)Sn(SPh)3 · W(CO)5 (IV). A similar treatment of complex III resulted in the formation of the ditungsten complex $ W_{2} $(CO)4(SePh)6 (V) with transfer of all chalcogenate groups from tin to tungsten. In reactions of complexes II and III with a $ Pt_{0} $ complex with phosphine and acetylene, ($ PPh_{3} $)2Pt($ Ph_{2} %$ C_{2} $), the chalcogenate groups are transferred from tin. Only the known Pt(II) complexes ($ PPh_{3} $)2Pt(EPh)2), where E= S (VI) or Se (VII). Molecular structures IV and V were characterized by X-ray diffraction. It has been found that the Mn-Sn bond in complex IV (2.5479(9) Å) is nearly the same length as that found earlier for complex II (2.5328(17) Å) and is substantially shorter than the sum of the covalent radii of Mn and Sn (2.78 Å). The Sn-S bond is noticeably lengthened (2.5217(11) Å) only for the S atom bound to tungsten (W-S, 2.5696(12) Å), while the other Sn-S bonds (2.4413(12) and 2.4291(12) Å) are virtually the same as in complex II (on average, 2.441 Å). Complex V contains the direct W-W bond (2.8153(16) Å) supplemented with four benzeneselenolate bridges in which the W-Se bonds (on average, 2.642(2) Å) are longer than the two terminal W-SePh bonds (2.571(2) Å). All the W-Se bonds are much shorter than the sum of the covalent radii of W and Se (2.82 Å). |
abstractGer |
Abstract Reactions of CpMn(CO)(NO)$ SnCl_{3} $ (I) with sodium benzenethiolate and sodium benzenesele-nolate gave orange crystals of the complexes CpMn(CO)(NO)Sn(EPh)3, where E = S (II) or Se (III). Treatment of complex II with photochemically generated W(CO)5(THF) yielded the adduct CpMn(CO)(NO)Sn(SPh)3 · W(CO)5 (IV). A similar treatment of complex III resulted in the formation of the ditungsten complex $ W_{2} $(CO)4(SePh)6 (V) with transfer of all chalcogenate groups from tin to tungsten. In reactions of complexes II and III with a $ Pt_{0} $ complex with phosphine and acetylene, ($ PPh_{3} $)2Pt($ Ph_{2} %$ C_{2} $), the chalcogenate groups are transferred from tin. Only the known Pt(II) complexes ($ PPh_{3} $)2Pt(EPh)2), where E= S (VI) or Se (VII). Molecular structures IV and V were characterized by X-ray diffraction. It has been found that the Mn-Sn bond in complex IV (2.5479(9) Å) is nearly the same length as that found earlier for complex II (2.5328(17) Å) and is substantially shorter than the sum of the covalent radii of Mn and Sn (2.78 Å). The Sn-S bond is noticeably lengthened (2.5217(11) Å) only for the S atom bound to tungsten (W-S, 2.5696(12) Å), while the other Sn-S bonds (2.4413(12) and 2.4291(12) Å) are virtually the same as in complex II (on average, 2.441 Å). Complex V contains the direct W-W bond (2.8153(16) Å) supplemented with four benzeneselenolate bridges in which the W-Se bonds (on average, 2.642(2) Å) are longer than the two terminal W-SePh bonds (2.571(2) Å). All the W-Se bonds are much shorter than the sum of the covalent radii of W and Se (2.82 Å). |
abstract_unstemmed |
Abstract Reactions of CpMn(CO)(NO)$ SnCl_{3} $ (I) with sodium benzenethiolate and sodium benzenesele-nolate gave orange crystals of the complexes CpMn(CO)(NO)Sn(EPh)3, where E = S (II) or Se (III). Treatment of complex II with photochemically generated W(CO)5(THF) yielded the adduct CpMn(CO)(NO)Sn(SPh)3 · W(CO)5 (IV). A similar treatment of complex III resulted in the formation of the ditungsten complex $ W_{2} $(CO)4(SePh)6 (V) with transfer of all chalcogenate groups from tin to tungsten. In reactions of complexes II and III with a $ Pt_{0} $ complex with phosphine and acetylene, ($ PPh_{3} $)2Pt($ Ph_{2} %$ C_{2} $), the chalcogenate groups are transferred from tin. Only the known Pt(II) complexes ($ PPh_{3} $)2Pt(EPh)2), where E= S (VI) or Se (VII). Molecular structures IV and V were characterized by X-ray diffraction. It has been found that the Mn-Sn bond in complex IV (2.5479(9) Å) is nearly the same length as that found earlier for complex II (2.5328(17) Å) and is substantially shorter than the sum of the covalent radii of Mn and Sn (2.78 Å). The Sn-S bond is noticeably lengthened (2.5217(11) Å) only for the S atom bound to tungsten (W-S, 2.5696(12) Å), while the other Sn-S bonds (2.4413(12) and 2.4291(12) Å) are virtually the same as in complex II (on average, 2.441 Å). Complex V contains the direct W-W bond (2.8153(16) Å) supplemented with four benzeneselenolate bridges in which the W-Se bonds (on average, 2.642(2) Å) are longer than the two terminal W-SePh bonds (2.571(2) Å). All the W-Se bonds are much shorter than the sum of the covalent radii of W and Se (2.82 Å). |
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container_issue |
12 |
title_short |
Synthesis and molecular structures of tris(thio- and selenophenyl)stannyl complexes of cyclopentadienylcarbonylnitrosylmanganese and their reaction products with tungsten carbony |
url |
https://dx.doi.org/10.1134/S1070328411110108 |
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Blokhin, A. I. Torubaev, Yu. V. Dobrokhotova, Zh. V. |
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score |
7.400222 |