Metal complexes in catalytic conversions of olefins. 4. Heterogenization of nickel complexes on chemically modified silochrome surface; activity and selectivity in ethylene dimerization

ISSN:
1573-9171
Source:
Springer Online Journal Archives 1860-2000
Topics:
Chemistry and Pharmacology
Notes:
Abstract When activated by Et2AlCl phosphine-containing homogeneous nickel complexes and their heterogenized analogs (HMC) formed on silochrome S-120 modified by NH2 and N(PPh2)2 groups differ significantly in their effectiveness in ethylene dimerization. The catalytic activity of Ni-HMC-Et2AlCl depends on how the HMC was formed. Ni-HMC-I obtained by ligand exchange on chemically modified silochrome is ∼5–15 times more effective than Ni-HMC-II synthesized from the gas phase. The selectivity in formation of α-olefins (σC4 + σC6) is ∼4–5 times higher in the presence of Ni-HMC than for its homogeneous analogs.
Type of Medium:
Electronic Resource
URL:
_version_ 1798297497155665920
autor Furman, D. B.
Ivanov, A. O.
Olenin, A. Yu.
Vasil'kov, A. Yu.
Munshieva, M. K.
Belyankin, A. Yu.
Lisichkin, G. V.
Sergeev, V. A.
Bragin, O. V.
autorsonst Furman, D. B.
Ivanov, A. O.
Olenin, A. Yu.
Vasil'kov, A. Yu.
Munshieva, M. K.
Belyankin, A. Yu.
Lisichkin, G. V.
Sergeev, V. A.
Bragin, O. V.
book_url http://dx.doi.org/10.1007/BF00959556
datenlieferant nat_lic_papers
hauptsatz hsatz_simple
identnr NLM192191845
issn 1573-9171
journal_name Russian chemical bulletin
materialart 1
notes Abstract When activated by Et2AlCl phosphine-containing homogeneous nickel complexes and their heterogenized analogs (HMC) formed on silochrome S-120 modified by NH2 and N(PPh2)2 groups differ significantly in their effectiveness in ethylene dimerization. The catalytic activity of Ni-HMC-Et2AlCl depends on how the HMC was formed. Ni-HMC-I obtained by ligand exchange on chemically modified silochrome is ∼5–15 times more effective than Ni-HMC-II synthesized from the gas phase. The selectivity in formation of α-olefins (σC4 + σC6) is ∼4–5 times higher in the presence of Ni-HMC than for its homogeneous analogs.
package_name Springer
publikationsjahr_anzeige 1990
publikationsjahr_facette 1990
publikationsjahr_intervall 8009:1990-1994
publikationsjahr_sort 1990
publisher Springer
reference 39 (1990), S. 448-451
search_space articles
shingle_author_1 Furman, D. B.
Ivanov, A. O.
Olenin, A. Yu.
Vasil'kov, A. Yu.
Munshieva, M. K.
Belyankin, A. Yu.
Lisichkin, G. V.
Sergeev, V. A.
Bragin, O. V.
shingle_author_2 Furman, D. B.
Ivanov, A. O.
Olenin, A. Yu.
Vasil'kov, A. Yu.
Munshieva, M. K.
Belyankin, A. Yu.
Lisichkin, G. V.
Sergeev, V. A.
Bragin, O. V.
shingle_author_3 Furman, D. B.
Ivanov, A. O.
Olenin, A. Yu.
Vasil'kov, A. Yu.
Munshieva, M. K.
Belyankin, A. Yu.
Lisichkin, G. V.
Sergeev, V. A.
Bragin, O. V.
shingle_author_4 Furman, D. B.
Ivanov, A. O.
Olenin, A. Yu.
Vasil'kov, A. Yu.
Munshieva, M. K.
Belyankin, A. Yu.
Lisichkin, G. V.
Sergeev, V. A.
Bragin, O. V.
shingle_catch_all_1 Furman, D. B.
Ivanov, A. O.
Olenin, A. Yu.
Vasil'kov, A. Yu.
Munshieva, M. K.
Belyankin, A. Yu.
Lisichkin, G. V.
Sergeev, V. A.
Bragin, O. V.
Metal complexes in catalytic conversions of olefins. 4. Heterogenization of nickel complexes on chemically modified silochrome surface; activity and selectivity in ethylene dimerization
Abstract When activated by Et2AlCl phosphine-containing homogeneous nickel complexes and their heterogenized analogs (HMC) formed on silochrome S-120 modified by NH2 and N(PPh2)2 groups differ significantly in their effectiveness in ethylene dimerization. The catalytic activity of Ni-HMC-Et2AlCl depends on how the HMC was formed. Ni-HMC-I obtained by ligand exchange on chemically modified silochrome is ∼5–15 times more effective than Ni-HMC-II synthesized from the gas phase. The selectivity in formation of α-olefins (σC4 + σC6) is ∼4–5 times higher in the presence of Ni-HMC than for its homogeneous analogs.
1573-9171
15739171
Springer
shingle_catch_all_2 Furman, D. B.
Ivanov, A. O.
Olenin, A. Yu.
Vasil'kov, A. Yu.
Munshieva, M. K.
Belyankin, A. Yu.
Lisichkin, G. V.
Sergeev, V. A.
Bragin, O. V.
Metal complexes in catalytic conversions of olefins. 4. Heterogenization of nickel complexes on chemically modified silochrome surface; activity and selectivity in ethylene dimerization
Abstract When activated by Et2AlCl phosphine-containing homogeneous nickel complexes and their heterogenized analogs (HMC) formed on silochrome S-120 modified by NH2 and N(PPh2)2 groups differ significantly in their effectiveness in ethylene dimerization. The catalytic activity of Ni-HMC-Et2AlCl depends on how the HMC was formed. Ni-HMC-I obtained by ligand exchange on chemically modified silochrome is ∼5–15 times more effective than Ni-HMC-II synthesized from the gas phase. The selectivity in formation of α-olefins (σC4 + σC6) is ∼4–5 times higher in the presence of Ni-HMC than for its homogeneous analogs.
1573-9171
15739171
Springer
shingle_catch_all_3 Furman, D. B.
Ivanov, A. O.
Olenin, A. Yu.
Vasil'kov, A. Yu.
Munshieva, M. K.
Belyankin, A. Yu.
Lisichkin, G. V.
Sergeev, V. A.
Bragin, O. V.
Metal complexes in catalytic conversions of olefins. 4. Heterogenization of nickel complexes on chemically modified silochrome surface; activity and selectivity in ethylene dimerization
Abstract When activated by Et2AlCl phosphine-containing homogeneous nickel complexes and their heterogenized analogs (HMC) formed on silochrome S-120 modified by NH2 and N(PPh2)2 groups differ significantly in their effectiveness in ethylene dimerization. The catalytic activity of Ni-HMC-Et2AlCl depends on how the HMC was formed. Ni-HMC-I obtained by ligand exchange on chemically modified silochrome is ∼5–15 times more effective than Ni-HMC-II synthesized from the gas phase. The selectivity in formation of α-olefins (σC4 + σC6) is ∼4–5 times higher in the presence of Ni-HMC than for its homogeneous analogs.
1573-9171
15739171
Springer
shingle_catch_all_4 Furman, D. B.
Ivanov, A. O.
Olenin, A. Yu.
Vasil'kov, A. Yu.
Munshieva, M. K.
Belyankin, A. Yu.
Lisichkin, G. V.
Sergeev, V. A.
Bragin, O. V.
Metal complexes in catalytic conversions of olefins. 4. Heterogenization of nickel complexes on chemically modified silochrome surface; activity and selectivity in ethylene dimerization
Abstract When activated by Et2AlCl phosphine-containing homogeneous nickel complexes and their heterogenized analogs (HMC) formed on silochrome S-120 modified by NH2 and N(PPh2)2 groups differ significantly in their effectiveness in ethylene dimerization. The catalytic activity of Ni-HMC-Et2AlCl depends on how the HMC was formed. Ni-HMC-I obtained by ligand exchange on chemically modified silochrome is ∼5–15 times more effective than Ni-HMC-II synthesized from the gas phase. The selectivity in formation of α-olefins (σC4 + σC6) is ∼4–5 times higher in the presence of Ni-HMC than for its homogeneous analogs.
1573-9171
15739171
Springer
shingle_title_1 Metal complexes in catalytic conversions of olefins. 4. Heterogenization of nickel complexes on chemically modified silochrome surface; activity and selectivity in ethylene dimerization
shingle_title_2 Metal complexes in catalytic conversions of olefins. 4. Heterogenization of nickel complexes on chemically modified silochrome surface; activity and selectivity in ethylene dimerization
shingle_title_3 Metal complexes in catalytic conversions of olefins. 4. Heterogenization of nickel complexes on chemically modified silochrome surface; activity and selectivity in ethylene dimerization
shingle_title_4 Metal complexes in catalytic conversions of olefins. 4. Heterogenization of nickel complexes on chemically modified silochrome surface; activity and selectivity in ethylene dimerization
sigel_instance_filter dkfz
geomar
wilbert
ipn
albert
fhp
source_archive Springer Online Journal Archives 1860-2000
timestamp 2024-05-06T10:08:55.428Z
titel Metal complexes in catalytic conversions of olefins. 4. Heterogenization of nickel complexes on chemically modified silochrome surface; activity and selectivity in ethylene dimerization
titel_suche Metal complexes in catalytic conversions of olefins. 4. Heterogenization of nickel complexes on chemically modified silochrome surface; activity and selectivity in ethylene dimerization
topic V
uid nat_lic_papers_NLM192191845