Dalton Transactions, volume 46, issue 35, pages 11790-11799

Hoveyda–Grubbs catalyst analogues bearing the derivatives of N-phenylpyrrol in the carbene ligand – structure, stability, activity and unique ruthenium–phenyl interactions

K Grudzień ¹

Bartosz Trzaskowski ²

Michał Smoleń ¹

Roman Gajda ¹

Krzysztof Woźniak ¹

Karol Grela ¹

Faculty of Chemistry, Biological and Chemical Research Centre, University of Warsaw, Żwirki I Wigury 101, 02-089 Warsaw, Poland |

Centre of New Technologies, University of Warsaw, S. Banacha 2c, 02-097 Warsaw, Poland |

Publication type: Journal Article

Publication date: 2017-08-10

Royal Society of Chemistry (RSC)

Journal: Dalton Transactions

scimago Q1

SJR: 0.697

CiteScore: 6.6

Impact factor: 3.5

ISSN: 14779226, 14779234

DOI: 10.1039/c7dt02180a

Copy DOI

PubMed ID: 28829469

Inorganic Chemistry

Abstract

N-Phenylpyrrole-2,6-diisopropylphenyl ruthenium complex and its perbrominated derivative are active in ring-closing metathesis at 80 °C, but inactive at room temperature.

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American Chemical Society (ACS)	American Chemical Society (ACS), 8, 44.44% American Chemical Society (ACS) 8 publications, 44.44%
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Beilstein-Institut	Beilstein-Institut, 1, 5.56% Beilstein-Institut 1 publication, 5.56%
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Publisher

Royal Society of Chemistry (RSC)

Journal

Dalton Transactions

scimago Q1

SJR

0.697

CiteScore

6.6

Impact factor

3.5

ISSN

14779226 (Print)

14779234 (Electronic)

Profiles

Grela, Karol

Hoveyda–Grubbs catalyst analogues bearing the derivatives of N-phenylpyrrol in the carbene ligand – structure, stability, activity and unique ruthenium–phenyl interactions

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