ACS Catalysis, volume 7, issue 6, pages 4115-4121
Rational and Then Serendipitous Formation of Aza Analogues of Hoveyda-Type Catalysts Containing a Chelating Ester Group Leading to a Polymerization Catalyst Family
Stefan Czarnocki
1
,
Izabela Czeluśniak
2
,
Tomasz Olszewski
3
,
Maura Malinska
1
,
Krzysztof Woźniak
1
,
Publication type: Journal Article
Publication date: 2017-05-16
Journal:
ACS Catalysis
Quartile SCImago
Q1
Quartile WOS
Q1
Impact factor: 12.9
ISSN: 21555435, 21555435
General Chemistry
Catalysis
Abstract
Analogues of the well-known Hoveyda–Grubbs catalyst bearing both a chelating ester function and a chelating nitrogen atom were obtained. These complexes behave differently depending on the character of the chelating amine. Complexes containing a secondary amine underwent unexpected spontaneous oxidation of the amine group, leading to the Schiff base analogues. In contrast, complexes containing a tertiary amine were prone to intramolecular cyclization in the presence of a base (Et3N). Probing the activity of such (pre)catalysts in ring-closing metathesis reactions (RCMs) revealed their dormant character and excellent thermo-switchability. In particular, complexes bearing an iminium nitrogen fragment were found to be very useful in a delayed ring-opening metathesis polymerization (ROMP) and were therefore commercialized.
Top-30
Citations by journals
1
2
|
|
Macromolecules
2 publications, 7.41%
|
|
Russian Chemical Reviews
2 publications, 7.41%
|
|
European Journal of Inorganic Chemistry
2 publications, 7.41%
|
|
Organometallics
2 publications, 7.41%
|
|
Progress in Polymer Science
1 publication, 3.7%
|
|
Coordination Chemistry Reviews
1 publication, 3.7%
|
|
Asian Journal of Organic Chemistry
1 publication, 3.7%
|
|
Journal of the American Chemical Society
1 publication, 3.7%
|
|
ACS Catalysis
1 publication, 3.7%
|
|
ACS Applied Polymer Materials
1 publication, 3.7%
|
|
Organic Process Research and Development
1 publication, 3.7%
|
|
Chemistry of Materials
1 publication, 3.7%
|
|
Faraday Discussions
1 publication, 3.7%
|
|
Molecules
1 publication, 3.7%
|
|
Catalysts
1 publication, 3.7%
|
|
New Journal of Chemistry
1 publication, 3.7%
|
|
Materials Chemistry Frontiers
1 publication, 3.7%
|
|
Polymer Chemistry
1 publication, 3.7%
|
|
Inorganics
1 publication, 3.7%
|
|
Dalton Transactions
1 publication, 3.7%
|
|
Journal of Organometallic Chemistry
1 publication, 3.7%
|
|
1
2
|
Citations by publishers
1
2
3
4
5
6
7
8
9
|
|
American Chemical Society (ACS)
9 publications, 33.33%
|
|
Royal Society of Chemistry (RSC)
5 publications, 18.52%
|
|
Wiley
4 publications, 14.81%
|
|
Elsevier
3 publications, 11.11%
|
|
Multidisciplinary Digital Publishing Institute (MDPI)
3 publications, 11.11%
|
|
Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii
2 publications, 7.41%
|
|
1
2
3
4
5
6
7
8
9
|
- We do not take into account publications 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":[2018,2019,2020,2021,2022,2023,2024],"ids":[0,0,0,0,0,0,0],"codes":[0,0,0,0,0,0,0],"imageUrls":["","","","","","",""],"datasets":[{"label":"Citations number","data":[6,1,5,4,2,6,3],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":["22.22","3.7","18.52","14.81","7.41","22.22","11.11"],"barThickness":null}]},"options":{"indexAxis":"x","maintainAspectRatio":true,"scales":{"y":{"ticks":{"precision":0,"autoSkip":false,"font":{"family":"Montserrat"},"color":"#000000"},"stacked":false},"x":{"ticks":{"stepSize":1,"precision":0,"font":{"family":"Montserrat"},"color":"#000000"},"stacked":false}},"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":["Macromolecules","Russian Chemical Reviews","European Journal of Inorganic Chemistry","Organometallics","Progress in Polymer Science","Coordination Chemistry Reviews","Asian Journal of Organic Chemistry","Journal of the American Chemical Society","ACS Catalysis","ACS Applied Polymer Materials","Organic Process Research and Development","Chemistry of Materials","Faraday Discussions","Molecules","Catalysts","New Journal of Chemistry","Materials Chemistry Frontiers","Polymer Chemistry","Inorganics","Dalton Transactions","Journal of Organometallic Chemistry"],"ids":[20817,23802,15359,1409,15618,13437,9409,4813,4873,25373,11058,6428,19474,1770,3739,1404,7063,11501,4005,8473,11834],"codes":[0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0],"imageUrls":["\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/9Mus3KG1Tkd7Bwaurt8H3RwWh0CxRlGoO6ng9UK1_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/MjH1ITP7lMYGxeqUZfkt2BnVLgjkk413jwBV97XX_medium.webp","\/storage\/images\/resized\/MjH1ITP7lMYGxeqUZfkt2BnVLgjkk413jwBV97XX_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/MjH1ITP7lMYGxeqUZfkt2BnVLgjkk413jwBV97XX_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp"],"datasets":[{"label":"","data":[2,2,2,2,1,1,1,1,1,1,1,1,1,1,1,1,1,1,1,1,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":[7.41,7.41,7.41,7.41,3.7,3.7,3.7,3.7,3.7,3.7,3.7,3.7,3.7,3.7,3.7,3.7,3.7,3.7,3.7,3.7,3.7],"barThickness":13}]},"options":{"indexAxis":"y","maintainAspectRatio":false,"scales":{"y":{"ticks":{"precision":0,"autoSkip":false,"font":{"family":"Montserrat"},"color":"#000000"},"stacked":false},"x":{"ticks":{"stepSize":null,"precision":0,"font":{"family":"Montserrat"},"color":"#000000"},"stacked":false}},"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":["American Chemical Society (ACS)","Royal Society of Chemistry (RSC)","Wiley","Elsevier","Multidisciplinary Digital Publishing Institute (MDPI)","Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii"],"ids":[40,123,11,17,202,9422],"codes":[0,0,0,0,0,0],"imageUrls":["\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/MjH1ITP7lMYGxeqUZfkt2BnVLgjkk413jwBV97XX_medium.webp","\/storage\/images\/resized\/9Mus3KG1Tkd7Bwaurt8H3RwWh0CxRlGoO6ng9UK1_medium.webp"],"datasets":[{"label":"","data":[9,5,4,3,3,2],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":[33.33,18.52,14.81,11.11,11.11,7.41],"barThickness":13}]},"options":{"indexAxis":"y","maintainAspectRatio":false,"scales":{"y":{"ticks":{"precision":0,"autoSkip":false,"font":{"family":"Montserrat"},"color":"#000000"},"stacked":false},"x":{"ticks":{"stepSize":null,"precision":0,"font":{"family":"Montserrat"},"color":"#000000"},"stacked":false}},"plugins":{"legend":{"position":"top","labels":{"font":{"family":"Montserrat"},"color":"#000000"}},"title":{"display":true,"text":"Publishers","font":{"size":24,"family":"Montserrat","weight":600},"color":"#000000"}}}},"yearsCitationsQuartiles":{"type":"bar","data":{"show":true,"labels":[2018,2019,2020,2021,2022,2023,2024],"ids":[],"codes":[],"imageUrls":[],"datasets":[{"label":"Q4","backgroundColor":"rgb(221,90,78)","data":[0,0,0,0,0,0,0],"percentage":["0","0","0","0","0","0","0"]},{"label":"Q3","backgroundColor":"rgb(251, 163,83)","data":[0,0,0,0,0,0,1],"percentage":["0","0","0","0","0","0","3.7"]},{"label":"Q2","backgroundColor":"rgb(232, 213, 89)","data":[2,0,0,0,1,2,1],"percentage":["7.41","0","0","0","3.7","7.41","3.7"]},{"label":"Q1","backgroundColor":"rgb(164, 207, 99)","data":[4,1,4,3,1,4,1],"percentage":["14.81","3.7","14.81","11.11","3.7","14.81","3.7"]},{"label":"Quartile not defined","backgroundColor":"#E5E7EB","data":[0,0,1,1,0,0,0],"percentage":["0","0","3.7","3.7","0","0","0"]}]},"options":{"indexAxis":"x","maintainAspectRatio":true,"scales":{"y":{"ticks":{"precision":0,"autoSkip":false,"font":{"family":"Montserrat"},"color":"#000000"},"stacked":true},"x":{"ticks":{"stepSize":1,"precision":0,"font":{"family":"Montserrat"},"color":"#000000"},"stacked":true}},"plugins":{"legend":{"position":"top","labels":{"font":{"family":"Montserrat"},"color":"#000000"}},"title":{"display":true,"text":"Citations quartiles by SCImago per year","font":{"size":24,"family":"Montserrat","weight":600},"color":"#000000"}}}},"yearsCitationsQuartilesWs":{"type":"bar","data":{"show":true,"labels":[2018,2019,2020,2021,2022,2023,2024],"ids":[],"codes":[],"imageUrls":[],"datasets":[{"label":"Q4","backgroundColor":"rgb(221,90,78)","data":[0,0,0,0,0,0,0],"percentage":["0","0","0","0","0","0","0"]},{"label":"Q3","backgroundColor":"rgb(251, 163,83)","data":[0,0,0,0,0,1,0],"percentage":["0","0","0","0","0","3.7","0"]},{"label":"Q2","backgroundColor":"rgb(232, 213, 89)","data":[2,0,0,2,1,3,2],"percentage":["7.41","0","0","7.41","3.7","11.11","7.41"]},{"label":"Q1","backgroundColor":"rgb(164, 207, 99)","data":[4,1,4,1,1,2,1],"percentage":["14.81","3.7","14.81","3.7","3.7","7.41","3.7"]},{"label":"Quartile not defined","backgroundColor":"#E5E7EB","data":[0,0,1,1,0,0,0],"percentage":["0","0","3.7","3.7","0","0","0"]}]},"options":{"indexAxis":"x","maintainAspectRatio":true,"scales":{"y":{"ticks":{"precision":0,"autoSkip":false,"font":{"family":"Montserrat"},"color":"#000000"},"stacked":true},"x":{"ticks":{"stepSize":1,"precision":0,"font":{"family":"Montserrat"},"color":"#000000"},"stacked":true}},"plugins":{"legend":{"position":"top","labels":{"font":{"family":"Montserrat"},"color":"#000000"}},"title":{"display":true,"text":"Citations quartiles by WoS per year","font":{"size":24,"family":"Montserrat","weight":600},"color":"#000000"}}}}}
Are you a researcher?
Create a profile to get free access to personal recommendations for colleagues and new articles.
Metrics
Cite this
GOST |
RIS |
BibTex |
MLA
Cite this
GOST
Copy
Czarnocki S. et al. Rational and Then Serendipitous Formation of Aza Analogues of Hoveyda-Type Catalysts Containing a Chelating Ester Group Leading to a Polymerization Catalyst Family // ACS Catalysis. 2017. Vol. 7. No. 6. pp. 4115-4121.
GOST all authors (up to 50)
Copy
Czarnocki S., Czeluśniak I., Olszewski T., Malinska M., Woźniak K., Grela K. Rational and Then Serendipitous Formation of Aza Analogues of Hoveyda-Type Catalysts Containing a Chelating Ester Group Leading to a Polymerization Catalyst Family // ACS Catalysis. 2017. Vol. 7. No. 6. pp. 4115-4121.
Cite this
RIS
Copy
TY - JOUR
DO - 10.1021/acscatal.7b00843
UR - https://doi.org/10.1021/acscatal.7b00843
TI - Rational and Then Serendipitous Formation of Aza Analogues of Hoveyda-Type Catalysts Containing a Chelating Ester Group Leading to a Polymerization Catalyst Family
T2 - ACS Catalysis
AU - Czeluśniak, Izabela
AU - Woźniak, Krzysztof
AU - Grela, Karol
AU - Czarnocki, Stefan
AU - Olszewski, Tomasz
AU - Malinska, Maura
PY - 2017
DA - 2017/05/16 00:00:00
PB - American Chemical Society (ACS)
SP - 4115-4121
IS - 6
VL - 7
SN - 2155-5435
SN - 2155-5435
ER -
Cite this
BibTex
Copy
@article{2017_Czarnocki,
author = {Izabela Czeluśniak and Krzysztof Woźniak and Karol Grela and Stefan Czarnocki and Tomasz Olszewski and Maura Malinska},
title = {Rational and Then Serendipitous Formation of Aza Analogues of Hoveyda-Type Catalysts Containing a Chelating Ester Group Leading to a Polymerization Catalyst Family},
journal = {ACS Catalysis},
year = {2017},
volume = {7},
publisher = {American Chemical Society (ACS)},
month = {may},
url = {https://doi.org/10.1021/acscatal.7b00843},
number = {6},
pages = {4115--4121},
doi = {10.1021/acscatal.7b00843}
}
Cite this
MLA
Copy
Czarnocki, Stefan, et al. “Rational and Then Serendipitous Formation of Aza Analogues of Hoveyda-Type Catalysts Containing a Chelating Ester Group Leading to a Polymerization Catalyst Family.” ACS Catalysis, vol. 7, no. 6, May. 2017, pp. 4115-4121. https://doi.org/10.1021/acscatal.7b00843.