Synthesis of carbosilane dendrimers based on tetrakis(phenylethynyl)silane
Тип публикации: Journal Article
Дата публикации: 1998-07-01
scimago Q3
wos Q2
БС2
SJR: 0.385
CiteScore: 4.1
Impact factor: 2.4
ISSN: 0022328X, 18728561
Materials Chemistry
Organic Chemistry
Biochemistry
Inorganic Chemistry
Physical and Theoretical Chemistry
Краткое описание
Carbosilane dendrimers of first to third generation were synthesized, using alkynylation/hydrosilation cycles with lithium phenylacetylide and dichloromethylsilane as building blocks and tetrakis(phenylethynyl)silane as a core molecule. The analysis of the 1H- and 13C-NMR, MALDI mass spectra and elemental analysis made it possible to obtain pure and unified dendrimers.
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ГОСТ
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KIM C., Kim M. K. Synthesis of carbosilane dendrimers based on tetrakis(phenylethynyl)silane // Journal of Organometallic Chemistry. 1998. Vol. 563. No. 1-2. pp. 43-51.
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KIM C., Kim M. K. Synthesis of carbosilane dendrimers based on tetrakis(phenylethynyl)silane // Journal of Organometallic Chemistry. 1998. Vol. 563. No. 1-2. pp. 43-51.
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TY - JOUR
DO - 10.1016/S0022-328X(98)00562-2
UR - https://doi.org/10.1016/S0022-328X(98)00562-2
TI - Synthesis of carbosilane dendrimers based on tetrakis(phenylethynyl)silane
T2 - Journal of Organometallic Chemistry
AU - KIM, CHUNGKYUN
AU - Kim, Moon Kyun
PY - 1998
DA - 1998/07/01
PB - Elsevier
SP - 43-51
IS - 1-2
VL - 563
SN - 0022-328X
SN - 1872-8561
ER -
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@article{1998_KIM,
author = {CHUNGKYUN KIM and Moon Kyun Kim},
title = {Synthesis of carbosilane dendrimers based on tetrakis(phenylethynyl)silane},
journal = {Journal of Organometallic Chemistry},
year = {1998},
volume = {563},
publisher = {Elsevier},
month = {jul},
url = {https://doi.org/10.1016/S0022-328X(98)00562-2},
number = {1-2},
pages = {43--51},
doi = {10.1016/S0022-328X(98)00562-2}
}
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MLA
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KIM, CHUNGKYUN, et al. “Synthesis of carbosilane dendrimers based on tetrakis(phenylethynyl)silane.” Journal of Organometallic Chemistry, vol. 563, no. 1-2, Jul. 1998, pp. 43-51. https://doi.org/10.1016/S0022-328X(98)00562-2.