Influence of solvent on the yield of singlet oxygen upon the chloride ion-catalyzed decomposition of dimethyldioxirane
Abstract The excitation yield of the singlet molecular oxygen 1$ Δ_{g} $ [φ(1$ O_{2} $)] in the reaction of the dimethyldioxirane with the chloride ion in benzene, acetone, methylene chloride, and acetonitrile solutions has been determined. The φ(1$ O_{2} $) value depends on the solvent nature and i...
Ausführliche Beschreibung
Autor*in: |
Kazakov, D. V. [verfasserIn] Ovchinnikov, M. Yu. [verfasserIn] Khursan, S. L. [verfasserIn] |
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Format: |
E-Artikel |
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Sprache: |
Englisch |
Erschienen: |
2011 |
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Schlagwörter: |
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Übergeordnetes Werk: |
Enthalten in: High energy chemistry - Dordrecht [u.a.] : Springer Science + Business Media B.V, 2000, 45(2011), 6 vom: Nov., Seite 459-464 |
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Übergeordnetes Werk: |
volume:45 ; year:2011 ; number:6 ; month:11 ; pages:459-464 |
Links: |
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DOI / URN: |
10.1134/S0018143911060099 |
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Katalog-ID: |
SPR012801046 |
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245 | 1 | 0 | |a Influence of solvent on the yield of singlet oxygen upon the chloride ion-catalyzed decomposition of dimethyldioxirane |
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520 | |a Abstract The excitation yield of the singlet molecular oxygen 1$ Δ_{g} $ [φ(1$ O_{2} $)] in the reaction of the dimethyldioxirane with the chloride ion in benzene, acetone, methylene chloride, and acetonitrile solutions has been determined. The φ(1$ O_{2} $) value depends on the solvent nature and is in the range 50–84%. Correlation between the value of the singlet oxygen yield and the Kamlet-Taft parameter (α) characterizing the acidity of the solvent as a hydrogen bond donor has been established: the higher the α value, the higher the 1$ O_{2} $ yield. | ||
650 | 4 | |a Singlet Oxygen |7 (dpeaa)DE-He213 | |
650 | 4 | |a High Energy Chemistry |7 (dpeaa)DE-He213 | |
650 | 4 | |a Singlet Oxygen Generation |7 (dpeaa)DE-He213 | |
650 | 4 | |a Tetrabutylammonium Salt |7 (dpeaa)DE-He213 | |
650 | 4 | |a Dioxirane |7 (dpeaa)DE-He213 | |
700 | 1 | |a Ovchinnikov, M. Yu. |e verfasserin |4 aut | |
700 | 1 | |a Khursan, S. L. |e verfasserin |4 aut | |
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10.1134/S0018143911060099 doi (DE-627)SPR012801046 (SPR)S0018143911060099-e DE-627 ger DE-627 rakwb eng 540 ASE 35.90 bkl 35.16 bkl Kazakov, D. V. verfasserin aut Influence of solvent on the yield of singlet oxygen upon the chloride ion-catalyzed decomposition of dimethyldioxirane 2011 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract The excitation yield of the singlet molecular oxygen 1$ Δ_{g} $ [φ(1$ O_{2} $)] in the reaction of the dimethyldioxirane with the chloride ion in benzene, acetone, methylene chloride, and acetonitrile solutions has been determined. The φ(1$ O_{2} $) value depends on the solvent nature and is in the range 50–84%. Correlation between the value of the singlet oxygen yield and the Kamlet-Taft parameter (α) characterizing the acidity of the solvent as a hydrogen bond donor has been established: the higher the α value, the higher the 1$ O_{2} $ yield. Singlet Oxygen (dpeaa)DE-He213 High Energy Chemistry (dpeaa)DE-He213 Singlet Oxygen Generation (dpeaa)DE-He213 Tetrabutylammonium Salt (dpeaa)DE-He213 Dioxirane (dpeaa)DE-He213 Ovchinnikov, M. Yu. verfasserin aut Khursan, S. L. verfasserin aut Enthalten in High energy chemistry Dordrecht [u.a.] : Springer Science + Business Media B.V, 2000 45(2011), 6 vom: Nov., Seite 459-464 (DE-627)334290848 (DE-600)2057146-X 1608-3148 nnns volume:45 year:2011 number:6 month:11 pages:459-464 https://dx.doi.org/10.1134/S0018143911060099 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_206 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_2056 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_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 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_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 35.90 ASE 35.16 ASE AR 45 2011 6 11 459-464 |
spelling |
10.1134/S0018143911060099 doi (DE-627)SPR012801046 (SPR)S0018143911060099-e DE-627 ger DE-627 rakwb eng 540 ASE 35.90 bkl 35.16 bkl Kazakov, D. V. verfasserin aut Influence of solvent on the yield of singlet oxygen upon the chloride ion-catalyzed decomposition of dimethyldioxirane 2011 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract The excitation yield of the singlet molecular oxygen 1$ Δ_{g} $ [φ(1$ O_{2} $)] in the reaction of the dimethyldioxirane with the chloride ion in benzene, acetone, methylene chloride, and acetonitrile solutions has been determined. The φ(1$ O_{2} $) value depends on the solvent nature and is in the range 50–84%. Correlation between the value of the singlet oxygen yield and the Kamlet-Taft parameter (α) characterizing the acidity of the solvent as a hydrogen bond donor has been established: the higher the α value, the higher the 1$ O_{2} $ yield. Singlet Oxygen (dpeaa)DE-He213 High Energy Chemistry (dpeaa)DE-He213 Singlet Oxygen Generation (dpeaa)DE-He213 Tetrabutylammonium Salt (dpeaa)DE-He213 Dioxirane (dpeaa)DE-He213 Ovchinnikov, M. Yu. verfasserin aut Khursan, S. L. verfasserin aut Enthalten in High energy chemistry Dordrecht [u.a.] : Springer Science + Business Media B.V, 2000 45(2011), 6 vom: Nov., Seite 459-464 (DE-627)334290848 (DE-600)2057146-X 1608-3148 nnns volume:45 year:2011 number:6 month:11 pages:459-464 https://dx.doi.org/10.1134/S0018143911060099 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_206 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_2056 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_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 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_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 35.90 ASE 35.16 ASE AR 45 2011 6 11 459-464 |
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10.1134/S0018143911060099 doi (DE-627)SPR012801046 (SPR)S0018143911060099-e DE-627 ger DE-627 rakwb eng 540 ASE 35.90 bkl 35.16 bkl Kazakov, D. V. verfasserin aut Influence of solvent on the yield of singlet oxygen upon the chloride ion-catalyzed decomposition of dimethyldioxirane 2011 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract The excitation yield of the singlet molecular oxygen 1$ Δ_{g} $ [φ(1$ O_{2} $)] in the reaction of the dimethyldioxirane with the chloride ion in benzene, acetone, methylene chloride, and acetonitrile solutions has been determined. The φ(1$ O_{2} $) value depends on the solvent nature and is in the range 50–84%. Correlation between the value of the singlet oxygen yield and the Kamlet-Taft parameter (α) characterizing the acidity of the solvent as a hydrogen bond donor has been established: the higher the α value, the higher the 1$ O_{2} $ yield. Singlet Oxygen (dpeaa)DE-He213 High Energy Chemistry (dpeaa)DE-He213 Singlet Oxygen Generation (dpeaa)DE-He213 Tetrabutylammonium Salt (dpeaa)DE-He213 Dioxirane (dpeaa)DE-He213 Ovchinnikov, M. Yu. verfasserin aut Khursan, S. L. verfasserin aut Enthalten in High energy chemistry Dordrecht [u.a.] : Springer Science + Business Media B.V, 2000 45(2011), 6 vom: Nov., Seite 459-464 (DE-627)334290848 (DE-600)2057146-X 1608-3148 nnns volume:45 year:2011 number:6 month:11 pages:459-464 https://dx.doi.org/10.1134/S0018143911060099 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_206 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_2056 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_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 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_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 35.90 ASE 35.16 ASE AR 45 2011 6 11 459-464 |
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10.1134/S0018143911060099 doi (DE-627)SPR012801046 (SPR)S0018143911060099-e DE-627 ger DE-627 rakwb eng 540 ASE 35.90 bkl 35.16 bkl Kazakov, D. V. verfasserin aut Influence of solvent on the yield of singlet oxygen upon the chloride ion-catalyzed decomposition of dimethyldioxirane 2011 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract The excitation yield of the singlet molecular oxygen 1$ Δ_{g} $ [φ(1$ O_{2} $)] in the reaction of the dimethyldioxirane with the chloride ion in benzene, acetone, methylene chloride, and acetonitrile solutions has been determined. The φ(1$ O_{2} $) value depends on the solvent nature and is in the range 50–84%. Correlation between the value of the singlet oxygen yield and the Kamlet-Taft parameter (α) characterizing the acidity of the solvent as a hydrogen bond donor has been established: the higher the α value, the higher the 1$ O_{2} $ yield. Singlet Oxygen (dpeaa)DE-He213 High Energy Chemistry (dpeaa)DE-He213 Singlet Oxygen Generation (dpeaa)DE-He213 Tetrabutylammonium Salt (dpeaa)DE-He213 Dioxirane (dpeaa)DE-He213 Ovchinnikov, M. Yu. verfasserin aut Khursan, S. L. verfasserin aut Enthalten in High energy chemistry Dordrecht [u.a.] : Springer Science + Business Media B.V, 2000 45(2011), 6 vom: Nov., Seite 459-464 (DE-627)334290848 (DE-600)2057146-X 1608-3148 nnns volume:45 year:2011 number:6 month:11 pages:459-464 https://dx.doi.org/10.1134/S0018143911060099 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_206 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_2056 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_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 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_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 35.90 ASE 35.16 ASE AR 45 2011 6 11 459-464 |
allfieldsSound |
10.1134/S0018143911060099 doi (DE-627)SPR012801046 (SPR)S0018143911060099-e DE-627 ger DE-627 rakwb eng 540 ASE 35.90 bkl 35.16 bkl Kazakov, D. V. verfasserin aut Influence of solvent on the yield of singlet oxygen upon the chloride ion-catalyzed decomposition of dimethyldioxirane 2011 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract The excitation yield of the singlet molecular oxygen 1$ Δ_{g} $ [φ(1$ O_{2} $)] in the reaction of the dimethyldioxirane with the chloride ion in benzene, acetone, methylene chloride, and acetonitrile solutions has been determined. The φ(1$ O_{2} $) value depends on the solvent nature and is in the range 50–84%. Correlation between the value of the singlet oxygen yield and the Kamlet-Taft parameter (α) characterizing the acidity of the solvent as a hydrogen bond donor has been established: the higher the α value, the higher the 1$ O_{2} $ yield. Singlet Oxygen (dpeaa)DE-He213 High Energy Chemistry (dpeaa)DE-He213 Singlet Oxygen Generation (dpeaa)DE-He213 Tetrabutylammonium Salt (dpeaa)DE-He213 Dioxirane (dpeaa)DE-He213 Ovchinnikov, M. Yu. verfasserin aut Khursan, S. L. verfasserin aut Enthalten in High energy chemistry Dordrecht [u.a.] : Springer Science + Business Media B.V, 2000 45(2011), 6 vom: Nov., Seite 459-464 (DE-627)334290848 (DE-600)2057146-X 1608-3148 nnns volume:45 year:2011 number:6 month:11 pages:459-464 https://dx.doi.org/10.1134/S0018143911060099 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_206 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_2056 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_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 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_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 35.90 ASE 35.16 ASE AR 45 2011 6 11 459-464 |
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Enthalten in High energy chemistry 45(2011), 6 vom: Nov., Seite 459-464 volume:45 year:2011 number:6 month:11 pages:459-464 |
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Singlet Oxygen High Energy Chemistry Singlet Oxygen Generation Tetrabutylammonium Salt Dioxirane |
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Kazakov, D. V. @@aut@@ Ovchinnikov, M. Yu. @@aut@@ Khursan, S. L. @@aut@@ |
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|
author |
Kazakov, D. V. |
spellingShingle |
Kazakov, D. V. ddc 540 bkl 35.90 bkl 35.16 misc Singlet Oxygen misc High Energy Chemistry misc Singlet Oxygen Generation misc Tetrabutylammonium Salt misc Dioxirane Influence of solvent on the yield of singlet oxygen upon the chloride ion-catalyzed decomposition of dimethyldioxirane |
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topic_title |
540 ASE 35.90 bkl 35.16 bkl Influence of solvent on the yield of singlet oxygen upon the chloride ion-catalyzed decomposition of dimethyldioxirane Singlet Oxygen (dpeaa)DE-He213 High Energy Chemistry (dpeaa)DE-He213 Singlet Oxygen Generation (dpeaa)DE-He213 Tetrabutylammonium Salt (dpeaa)DE-He213 Dioxirane (dpeaa)DE-He213 |
topic |
ddc 540 bkl 35.90 bkl 35.16 misc Singlet Oxygen misc High Energy Chemistry misc Singlet Oxygen Generation misc Tetrabutylammonium Salt misc Dioxirane |
topic_unstemmed |
ddc 540 bkl 35.90 bkl 35.16 misc Singlet Oxygen misc High Energy Chemistry misc Singlet Oxygen Generation misc Tetrabutylammonium Salt misc Dioxirane |
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ddc 540 bkl 35.90 bkl 35.16 misc Singlet Oxygen misc High Energy Chemistry misc Singlet Oxygen Generation misc Tetrabutylammonium Salt misc Dioxirane |
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Influence of solvent on the yield of singlet oxygen upon the chloride ion-catalyzed decomposition of dimethyldioxirane |
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title_full |
Influence of solvent on the yield of singlet oxygen upon the chloride ion-catalyzed decomposition of dimethyldioxirane |
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Kazakov, D. V. |
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High energy chemistry |
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Kazakov, D. V. Ovchinnikov, M. Yu. Khursan, S. L. |
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540 ASE 35.90 bkl 35.16 bkl |
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Kazakov, D. V. |
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10.1134/S0018143911060099 |
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verfasserin |
title_sort |
influence of solvent on the yield of singlet oxygen upon the chloride ion-catalyzed decomposition of dimethyldioxirane |
title_auth |
Influence of solvent on the yield of singlet oxygen upon the chloride ion-catalyzed decomposition of dimethyldioxirane |
abstract |
Abstract The excitation yield of the singlet molecular oxygen 1$ Δ_{g} $ [φ(1$ O_{2} $)] in the reaction of the dimethyldioxirane with the chloride ion in benzene, acetone, methylene chloride, and acetonitrile solutions has been determined. The φ(1$ O_{2} $) value depends on the solvent nature and is in the range 50–84%. Correlation between the value of the singlet oxygen yield and the Kamlet-Taft parameter (α) characterizing the acidity of the solvent as a hydrogen bond donor has been established: the higher the α value, the higher the 1$ O_{2} $ yield. |
abstractGer |
Abstract The excitation yield of the singlet molecular oxygen 1$ Δ_{g} $ [φ(1$ O_{2} $)] in the reaction of the dimethyldioxirane with the chloride ion in benzene, acetone, methylene chloride, and acetonitrile solutions has been determined. The φ(1$ O_{2} $) value depends on the solvent nature and is in the range 50–84%. Correlation between the value of the singlet oxygen yield and the Kamlet-Taft parameter (α) characterizing the acidity of the solvent as a hydrogen bond donor has been established: the higher the α value, the higher the 1$ O_{2} $ yield. |
abstract_unstemmed |
Abstract The excitation yield of the singlet molecular oxygen 1$ Δ_{g} $ [φ(1$ O_{2} $)] in the reaction of the dimethyldioxirane with the chloride ion in benzene, acetone, methylene chloride, and acetonitrile solutions has been determined. The φ(1$ O_{2} $) value depends on the solvent nature and is in the range 50–84%. Correlation between the value of the singlet oxygen yield and the Kamlet-Taft parameter (α) characterizing the acidity of the solvent as a hydrogen bond donor has been established: the higher the α value, the higher the 1$ O_{2} $ yield. |
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6 |
title_short |
Influence of solvent on the yield of singlet oxygen upon the chloride ion-catalyzed decomposition of dimethyldioxirane |
url |
https://dx.doi.org/10.1134/S0018143911060099 |
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author2 |
Ovchinnikov, M. Yu Khursan, S. L. |
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Ovchinnikov, M. Yu Khursan, S. L. |
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doi_str |
10.1134/S0018143911060099 |
up_date |
2024-07-03T15:25:44.126Z |
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score |
7.4003124 |