[en] Ruthenium-N-heterocyclic carbene complexes with the generic formula [RuHCl(CO)(NHC)(PCy3)] exhibit a high catalytic activity toward the (E)-selective silylative coupling of divinyl-substituted double-decker silsesquioxanes with two distinctly substituted styrenes. This process leads to a novel class of unsymmetrically functionalized silsesquioxane derivatives.
Disciplines :
Chemistry
Author, co-author :
Zak, Patrycja; Department of Organometallic Chemistry, Faculty of Chemistry, Adam Mickiewicz University in Poznan, Umultowska 89B, Poznan, Poland
Delaude, Lionel ; Université de Liège - ULiège > Département de chimie (sciences) > Chimie organométallique et catalyse homogène
Dudziec, Beata; Department of Organometallic Chemistry, Faculty of Chemistry, Adam Mickiewicz University in Poznan, Umultowska 89B, Poznan, Poland, Centre for Advanced Technologies, Adam Mickiewicz University in Poznan, Umultowska 89C, Poznan, Poland
Marciniec, Bogdan; Department of Organometallic Chemistry, Faculty of Chemistry, Adam Mickiewicz University in Poznan, Umultowska 89B, Poznan, Poland, Centre for Advanced Technologies, Adam Mickiewicz University in Poznan, Umultowska 89C, Poznan, Poland
Language :
English
Title :
N-Heterocyclic carbene-based ruthenium-hydride catalysts for the synthesis of unsymmetrically functionalized double-decker silsesquioxanes
Publication date :
2018
Journal title :
Chemical Communications
ISSN :
1359-7345
eISSN :
1364-548X
Publisher :
Royal Society of Chemistry, Cambridge, United Kingdom
P. D. Lickiss F. Rataboul Adv. Organomet. Chem. 2008 57 1 116
D. B. Cordes P. D. Lickiss F. Rataboul Chem. Rev. 2010 110 2081 2173
L. Li L. Xue S. Feng H. Liu Inorg. Chim. Acta 2013 407 269 273
Y. Liu W. Yang H. Liu Chem.-Eur. J. 2015 21 4731 4738
L. Xue L. Li S. Feng H. Liu J. Organomet. Chem. 2015 783 49 54
M. Seino T. Hayakawa Y. Ishida M. Kakimoto K. Watanabe H. Oikawa Macromolecules 2006 39 3473 3475
Y. Morimoto, K. Watanabe, N. Ootake, J. Inagaki, K. Yoshida and K. Ohguma, US Pat., 7169873B2, 2007
J. Espinas J. D. A. Pelletier E. Abou-Hamad L. Emsley J.-M. Basset Organometallics 2012 31 7610 7617
N. Liu K. Wei L. Wang S. Zheng Polym. Chem. 2016 7 1158 1167
K. Mituła J. Duszczak D. Brzakalski B. Dudziec M. Kubicki B. Marciniec Chem. Commun. 2017 53 10370 10373
A. C. Kucuk J. Matsui T. Miyashita RSC Adv. 2018 8 2148 2156
Applications of Polyhedral Oligomeric Silsesquioxanes, in Advances in Silicon Science, ed., C. Hartmann-Thompson, Springer, Dordrecht, 2011, vol. 3
W. Zhang A. H. E. Müller Prog. Polym. Sci. 2013 38 1121 1162
Q. Ye H. Zhou J. Xu Chem.-Asian J. 2016 11 1322 1337
B. Dudziec B. Marciniec Curr. Org. Chem. 2017 21 2794 2813
V. Ervithayasuporn X. Wang Y. Kawakami Chem. Commun. 2009 5130 5132
B. Seurer V. Vij T. Haddad J. M. Mabry A. Lee Macromolecules 2010 43 9337 9347
V. Ervithayasuporn R. Sodkhomkhum T. Teerawatananond C. Phurat P. Phinyocheep E. Somsook T. Osotchan Eur. J. Inorg. Chem. 2013 3292 3296
Q. Jiang W. Zhang J. Hao Y. Wei J. Mu Z. Jiang J. Mater. Chem. C 2015 3 11729 11734
Y. Wei Q. Jiang J. Hao J. Mu Polym. Adv. Technol. 2017 28 516 523
P. Zak B. Dudziec M. Kubicki B. Marciniec Chem.-Eur. J. 2014 20 9387 9393
P. Zak M. Majchrzak G. Wilkowski B. Dudziec M. Dutkiewicz B. Marciniec RSC Adv. 2016 6 10054 10063
P. Zak B. Dudziec M. Dutkiewicz M. Ludwiczak B. Marciniec M. Nowicki J. Polym. Sci., Part A: Polym. Chem. 2016 54 1044 1055
P. Zak D. Frackowiak M. Grzelak M. Bołt M. Kubicki B. Marciniec Adv. Synth. Catal. 2016 358 3265 3276
M. Walczak R. Januszewski M. Majchrzak M. Kubicki B. Dudziec B. Marciniec New J. Chem. 2017 41 3290 3296
J. Kaźmierczak K. Kuciński G. Hreczycho Inorg. Chem. 2017 56 9337 9342
J. Kaźmierczak K. Kuciński G. Hreczycho Organometallics 2017 36 3854 3859
J. Kaźmierczak K. Kuciński H. Stachowiak G. Hreczycho Chem.-Eur. J. 2018 24 2509 2514
M. Seino Y. Kawakami Polym. J. 2004 36 422 429
R. M. Laine J. Mater. Chem. 2005 15 3725 3744
M. Dutkiewicz H. Maciejewski B. Marciniec J. Karasiewicz Organometallics 2011 30 2149 2153
J. H. Jung J. C. Furgal T. Goodson T. Mizumo M. Schwartz K. Chou J. F. Vonet R. M. Laine Chem. Mater. 2012 24 1883 1895
X. H. Yang T. Giovenzana B. Feild G. E. Jabbour A. Sellinger J. Mater. Chem. 2012 22 12689 12694
M. Arisawa Y. Terada K. Takahashi M. Nakagawa A. Nishida J. Org. Chem. 2006 71 4255 4261
N. J. Beach U. L. Dharmasena S. D. Drouin D. E. Fogg Adv. Synth. Catal. 2008 350 773 777
Y. Mutoh Y. Mohara S. Saito Org. Lett. 2017 19 5204 5207
B. Marciniec C. Pietraszuk Curr. Org. Chem. 2003 7 691 735
B. Marciniec Coord. Chem. Rev. 2005 249 2374 2390
B. Marciniec and C. Pietraszuk, in Green Metathesis Chemistry. Great Challenges in Synthesis Catalysis and Nanotechnology, ed., V. Dragutan, A. Demonceau, I. Dragutan, and, E. S. Finkelshtein, Springer, Dordrecht, 2010, pp. 157-171
C. Pietraszuk, P. Pawluć and B. Marciniec, in Handbook of Metathesis, ed., R. Grubbs, and, D. J. O'Leary, Wiley-VCH, Weinheim, 2nd edn, 2015, vol. 2, ch. 9, pp. 583-631
P. Zak M. Kubicki B. Marciniec S. Rogalski C. Pietraszuk D. Frackowiak Dalton Trans. 2014 43 7911 7916
J. A. M. Lummiss C. S. Higman D. L. Fyson R. McDonald D. E. Fogg Chem. Sci. 2015 6 6739 6746
B. Marciniec C. Pietraszuk Organometallics 1997 16 4320 4326
B. Marciniec S. Kostera B. Wyrzykiewicz P. Pawluć Dalton Trans. 2015 44 782 786