Chemistry - A European Journal, volume 26, issue 50, pages 11404-11407
Organoboron Derivatives of Stereoregular Phenylcyclosilsesquioxanes
Drozdov Fedor V
2
,
Vysochinskaya Yulia S
1, 2
,
Peregudov A. S.
1
,
Dolgushin Fedor
1, 3
,
Muzafarov Aziz M.
1, 2
Publication type: Journal Article
Publication date: 2020-08-11
Journal:
Chemistry - A European Journal
Quartile SCImago
Q1
Quartile WOS
Q2
Impact factor: 4.3
ISSN: 09476539, 15213765
General Chemistry
Catalysis
Organic Chemistry
Abstract
This study presents the synthesis of organoboron derivatives of stereoregular 4‐, 6‐, and 12‐unit phenylcyclosilsesquioxanes. All compounds obtained were isolated in good yields (70–80 %) and were fully characterized by 1H, 13C, 29Si, 11B NMR, IR spectroscopy, HRMS ESI, and elemental microanalysis. The structure of the key modifier, obtained for the first time, 4‐(tetramethyl‐1,3,2‐dioxaborolan‐2‐yl)phenyl) dimethylvinylsilane, was also confirmed by single‐crystal XRD.
Citations by journals
|
1
2
|
|
|
Polymers
|
Polymers
2 publications, 28.57%
|
|
Reaction Chemistry and Engineering
|
Reaction Chemistry and Engineering
1 publication, 14.29%
|
|
Molecules
|
Molecules
1 publication, 14.29%
|
|
Journal of Organometallic Chemistry
|
Journal of Organometallic Chemistry
1 publication, 14.29%
|
|
Dalton Transactions
|
Dalton Transactions
1 publication, 14.29%
|
|
Journal of Organic Chemistry
|
Journal of Organic Chemistry
1 publication, 14.29%
|
|
1
2
|
Citations by publishers
|
1
2
3
|
|
|
Multidisciplinary Digital Publishing Institute (MDPI)
|
Multidisciplinary Digital Publishing Institute (MDPI)
3 publications, 42.86%
|
|
Royal Society of Chemistry (RSC)
|
Royal Society of Chemistry (RSC)
2 publications, 28.57%
|
|
Elsevier
|
Elsevier
1 publication, 14.29%
|
|
American Chemical Society (ACS)
|
American Chemical Society (ACS)
1 publication, 14.29%
|
|
1
2
3
|
- We do not take into account publications that without a DOI.
- Statistics recalculated only for publications connected to researchers, organizations and labs registered on the platform.
- Statistics recalculated weekly.
{"yearsCitations":{"type":"bar","data":{"show":true,"labels":[2021,2022,2023],"ids":[0,0,0],"codes":[0,0,0],"imageUrls":["","",""],"datasets":[{"label":"Citations number","data":[1,4,2],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6"],"percentage":["14.29","57.14","28.57"],"barThickness":null}]},"options":{"indexAxis":"x","maintainAspectRatio":true,"scales":{"y":{"ticks":{"precision":0,"autoSkip":false,"font":{"family":"Montserrat"},"color":"#000000"}},"x":{"ticks":{"stepSize":1,"precision":0,"font":{"family":"Montserrat"},"color":"#000000"}}},"plugins":{"legend":{"position":"top","labels":{"font":{"family":"Montserrat"},"color":"#000000"}},"title":{"display":true,"text":"Citations per year","font":{"size":24,"family":"Montserrat","weight":600},"color":"#000000"}}}},"journals":{"type":"bar","data":{"show":true,"labels":["Polymers","Reaction Chemistry and Engineering","Molecules","Journal of Organometallic Chemistry","Dalton Transactions","Journal of Organic Chemistry"],"ids":[11204,20057,1770,11834,8473,8697],"codes":[0,0,0,0,0,0],"imageUrls":["\/storage\/images\/resized\/MjH1ITP7lMYGxeqUZfkt2BnVLgjkk413jwBV97XX_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/MjH1ITP7lMYGxeqUZfkt2BnVLgjkk413jwBV97XX_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp"],"datasets":[{"label":"","data":[2,1,1,1,1,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":[28.57,14.29,14.29,14.29,14.29,14.29],"barThickness":13}]},"options":{"indexAxis":"y","maintainAspectRatio":false,"scales":{"y":{"ticks":{"precision":0,"autoSkip":false,"font":{"family":"Montserrat"},"color":"#000000"}},"x":{"ticks":{"stepSize":null,"precision":0,"font":{"family":"Montserrat"},"color":"#000000"}}},"plugins":{"legend":{"position":"top","labels":{"font":{"family":"Montserrat"},"color":"#000000"}},"title":{"display":true,"text":"Journals","font":{"size":24,"family":"Montserrat","weight":600},"color":"#000000"}}}},"publishers":{"type":"bar","data":{"show":true,"labels":["Multidisciplinary Digital Publishing Institute (MDPI)","Royal Society of Chemistry (RSC)","Elsevier","American Chemical Society (ACS)"],"ids":[202,123,17,40],"codes":[0,0,0,0],"imageUrls":["\/storage\/images\/resized\/MjH1ITP7lMYGxeqUZfkt2BnVLgjkk413jwBV97XX_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp"],"datasets":[{"label":"","data":[3,2,1,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":[42.86,28.57,14.29,14.29],"barThickness":13}]},"options":{"indexAxis":"y","maintainAspectRatio":false,"scales":{"y":{"ticks":{"precision":0,"autoSkip":false,"font":{"family":"Montserrat"},"color":"#000000"}},"x":{"ticks":{"stepSize":null,"precision":0,"font":{"family":"Montserrat"},"color":"#000000"}}},"plugins":{"legend":{"position":"top","labels":{"font":{"family":"Montserrat"},"color":"#000000"}},"title":{"display":true,"text":"Publishers","font":{"size":24,"family":"Montserrat","weight":600},"color":"#000000"}}}}}
Metrics
Cite this
GOST |
RIS |
BibTex |
MLA
Cite this
GOST
Copy
Anisimov A. A. et al. Organoboron Derivatives of Stereoregular Phenylcyclosilsesquioxanes // Chemistry - A European Journal. 2020. Vol. 26. No. 50. pp. 11404-11407.
GOST all authors (up to 50)
Copy
Anisimov A. A., Drozdov F. V., Vysochinskaya Y. S., Minyaylo E. O., Peregudov A. S., Dolgushin F., Shchegolikhina O. I., Muzafarov A. M. Organoboron Derivatives of Stereoregular Phenylcyclosilsesquioxanes // Chemistry - A European Journal. 2020. Vol. 26. No. 50. pp. 11404-11407.
Cite this
RIS
Copy
TY - JOUR
DO - 10.1002/chem.202001676
UR - https://doi.org/10.1002%2Fchem.202001676
TI - Organoboron Derivatives of Stereoregular Phenylcyclosilsesquioxanes
T2 - Chemistry - A European Journal
AU - Vysochinskaya, Yulia S
AU - Minyaylo, Ekaterina O
AU - Anisimov, Anton A.
AU - Shchegolikhina, Olga I.
AU - Drozdov, Fedor V
AU - Peregudov, A. S.
AU - Dolgushin, Fedor
AU - Muzafarov, Aziz M.
PY - 2020
DA - 2020/08/11 00:00:00
PB - Wiley
SP - 11404-11407
IS - 50
VL - 26
SN - 0947-6539
SN - 1521-3765
ER -
Cite this
BibTex
Copy
@article{2020_Anisimov,
author = {Yulia S Vysochinskaya and Ekaterina O Minyaylo and Anton A. Anisimov and Olga I. Shchegolikhina and Fedor V Drozdov and A. S. Peregudov and Fedor Dolgushin and Aziz M. Muzafarov},
title = {Organoboron Derivatives of Stereoregular Phenylcyclosilsesquioxanes},
journal = {Chemistry - A European Journal},
year = {2020},
volume = {26},
publisher = {Wiley},
month = {aug},
url = {https://doi.org/10.1002%2Fchem.202001676},
number = {50},
pages = {11404--11407},
doi = {10.1002/chem.202001676}
}
Cite this
MLA
Copy
Anisimov, Anton A., et al. “Organoboron Derivatives of Stereoregular Phenylcyclosilsesquioxanes.” Chemistry - A European Journal, vol. 26, no. 50, Aug. 2020, pp. 11404-11407. https://doi.org/10.1002%2Fchem.202001676.