N-heterocyclic silylenes as powerful steering ligands in catalysis
The present review highlights the role of N-heterocyclic silylene (NHSi) ligands, the silicon analogues of N-heterocyclic carbenes (NHCs), utilized in various catalytic organic transformations. The application of such novel ligands coordinated by different metal sites offers massive opportunities in...
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Published in | Journal of organometallic chemistry Vol. 829; pp. 2 - 10 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
Elsevier B.V
01.02.2017
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Abstract | The present review highlights the role of N-heterocyclic silylene (NHSi) ligands, the silicon analogues of N-heterocyclic carbenes (NHCs), utilized in various catalytic organic transformations. The application of such novel ligands coordinated by different metal sites offers massive opportunities in organic synthesis. Despite significant advances in the synthesis of NHSi-based metal complexes, the use of these compounds in organic methodologies is still in its initial stages. Since NHSi ligands promote the σ donor-ability of phosphines and even that of NHCs, they can facilitate catalytic events by lowering the energy barrier of the rate limiting steps such as oxidative additions. This encourages scientists to utilize NHSi-metal complexes in exploiting catalyzed reactions and to revisit and improve various existing organic methodologies. This is demonstrated in several showcases of organic transformations including the Heck coupling, Suzuki coupling, alkyne and ketone hydrosilylation, amide reduction, cyclotrimerization of alkynes (in the absence and the presence of an organo cyanide), and Sonogashira cross-coupling reactions. The latter represents a novel and unexpected steering function of NHSi-based systems in homogeneous catalysis.
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•Synthesis and catalytic performance of monodentate, bidentate, and tridentate NHSi-transition metal complexes.•Stronger σ donor strength of NHSi ligands in comparison to NHCs and phosphines.•Catalytic performances of transition metal NHSi complexes. |
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AbstractList | The present review highlights the role of N-heterocyclic silylene (NHSi) ligands, the silicon analogues of N-heterocyclic carbenes (NHCs), utilized in various catalytic organic transformations. The application of such novel ligands coordinated by different metal sites offers massive opportunities in organic synthesis. Despite significant advances in the synthesis of NHSi-based metal complexes, the use of these compounds in organic methodologies is still in its initial stages. Since NHSi ligands promote the σ donor-ability of phosphines and even that of NHCs, they can facilitate catalytic events by lowering the energy barrier of the rate limiting steps such as oxidative additions. This encourages scientists to utilize NHSi-metal complexes in exploiting catalyzed reactions and to revisit and improve various existing organic methodologies. This is demonstrated in several showcases of organic transformations including the Heck coupling, Suzuki coupling, alkyne and ketone hydrosilylation, amide reduction, cyclotrimerization of alkynes (in the absence and the presence of an organo cyanide), and Sonogashira cross-coupling reactions. The latter represents a novel and unexpected steering function of NHSi-based systems in homogeneous catalysis.
[Display omitted]
•Synthesis and catalytic performance of monodentate, bidentate, and tridentate NHSi-transition metal complexes.•Stronger σ donor strength of NHSi ligands in comparison to NHCs and phosphines.•Catalytic performances of transition metal NHSi complexes. |
Author | Raoufmoghaddam, Saeed Zhou, Yu-Peng Wang, Yuwen Driess, Matthias |
Author_xml | – sequence: 1 givenname: Saeed surname: Raoufmoghaddam fullname: Raoufmoghaddam, Saeed – sequence: 2 givenname: Yu-Peng surname: Zhou fullname: Zhou, Yu-Peng – sequence: 3 givenname: Yuwen surname: Wang fullname: Wang, Yuwen – sequence: 4 givenname: Matthias surname: Driess fullname: Driess, Matthias email: matthias.driess@tu-berlin.de |
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Cites_doi | 10.1002/anie.200804993 10.1021/cr1003503 10.1002/anie.201200632 10.1039/c3cs60146c 10.1039/C4RA14417A 10.1021/ja910305p 10.1021/cr5002782 10.1021/ja062928i 10.1246/cl.2013.286 10.1016/j.ccr.2015.04.008 10.1021/ja106458p 10.1002/ange.19770891116 10.1002/zaac.200800131 10.1021/ja402480v 10.1002/anie.201106131 10.1039/C5SC02855H 10.1002/anie.197707851 10.1002/anie.201409739 10.1021/om050010e 10.1039/c1cs15071e 10.1002/anie.201205570 10.1021/ja9091374 10.1021/om500966t 10.1002/anie.200703883 10.1039/c1cs15088j 10.1039/c2cs35102a 10.1021/ja00070a047 10.1002/anie.201202175 10.1021/ar700028b 10.1021/ja408137t 10.1002/chem.201203072 10.1039/C3QI00079F 10.1039/b108132b 10.1039/b711132k 10.1071/CH13196 10.1021/cr050992x 10.1021/cr900074m 10.1038/nature13384 |
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Keywords | Silylenes Hydrosilylation Pincer ligands Silicon analogues of carbenes Homogeneous catalysis |
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References | Sen, Roesky, Stern, Henn, Stalke (bib23) 2010; 132 Neumann, Pfaltz (bib21) 2005; 24 Fortman, Nolan (bib2) 2011; 40 Hopkinson, Richter, Schedler, Glorius (bib1) 2014; 510 Someya, Haberberger, Wang, Enthaler, Inoue (bib12) 2013; 42 Blom, Gallego, Driess (bib11) 2014; 1 Driess, Yao, Brym, van Wuellen, Lentz (bib22) 2006; 128 Zhang, Liu, Shi, Ren, Ding, Roesky (bib26) 2008; 634 Wang, Inoue, Irran, Driess (bib33) 2012; 51 Hahn, Jahnke (bib3) 2008; 47 Meltzer, Inoue, Praesang, Driess (bib24) 2010; 132 Blom, Stoelzel, Driess (bib19) 2013; 19 Chinchilla, Najera (bib37) 2011; 40 Blom, Enthaler, Inoue, Irran, Driess (bib27) 2013; 135 Wang, Inoue, Yao, Driess (bib29) 2010; 132 Tan, Enthaler, Inoue, Blom, Driess (bib9) 2015; 54 Diez-Gonzalez, Marion, Nolan (bib5) 2009; 109 Metsänen, Gallego, Szilvási, Driess, Oestreich (bib10) 2015; 6 Benedek, Szilvasi (bib25) 2015; 5 Gallego, Inoue, Blom, Driess (bib38) 2014; 33 Nelson, Nolan (bib4) 2013; 42 Valente, Calimsiz, Hoi, Mallik, Sayah, Organ (bib7) 2012; 51 Wang, Inoue, Enthaler, Driess (bib30) 2012; 51 Schneider, Finger, Haferkemper, Bellemin-Laponnaz, Hofmann, Gade (bib13) 2009; 48 Waterman, Hayes, Tilley (bib14) 2007; 40 Stoelzel, Praesang, Blom, Driess (bib28) 2013; 66 Alvarez-Rodriguez, Cabeza, Garcia-Alvarez, Polo (bib16) 2015; 300 Schmid, Welz (bib17) 1977; 16 Brueck, Gallego, Wang, Irran, Driess, Hartwig (bib34) 2012; 51 Marion, Nolan (bib6) 2008; 37 Velazquez, Verpoort (bib8) 2012; 41 Chinchilla, Najera (bib36) 2007; 107 Grumbine, Tilley, Arnold, Rheingold (bib20) 1993; 115 Gunanathan, Milstein (bib31) 2014; 114 Furstner, Krause, Lehmann (bib18) 2001 Choi, MacArthur, Brookhart, Goldman (bib32) 2011; 111 Gallego, Brueck, Irran, Meier, Kaupp, Driess, Hartwig (bib35) 2013; 135 Schmid, Welz (bib15) 1977; 89 Sen (10.1016/j.jorganchem.2016.07.014_bib23) 2010; 132 Wang (10.1016/j.jorganchem.2016.07.014_bib30) 2012; 51 Schmid (10.1016/j.jorganchem.2016.07.014_bib15) 1977; 89 Hahn (10.1016/j.jorganchem.2016.07.014_bib3) 2008; 47 Zhang (10.1016/j.jorganchem.2016.07.014_bib26) 2008; 634 Marion (10.1016/j.jorganchem.2016.07.014_bib6) 2008; 37 Chinchilla (10.1016/j.jorganchem.2016.07.014_bib37) 2011; 40 Wang (10.1016/j.jorganchem.2016.07.014_bib33) 2012; 51 Velazquez (10.1016/j.jorganchem.2016.07.014_bib8) 2012; 41 Tan (10.1016/j.jorganchem.2016.07.014_bib9) 2015; 54 Valente (10.1016/j.jorganchem.2016.07.014_bib7) 2012; 51 Choi (10.1016/j.jorganchem.2016.07.014_bib32) 2011; 111 Driess (10.1016/j.jorganchem.2016.07.014_bib22) 2006; 128 Meltzer (10.1016/j.jorganchem.2016.07.014_bib24) 2010; 132 Wang (10.1016/j.jorganchem.2016.07.014_bib29) 2010; 132 Furstner (10.1016/j.jorganchem.2016.07.014_bib18) 2001 Chinchilla (10.1016/j.jorganchem.2016.07.014_bib36) 2007; 107 Brueck (10.1016/j.jorganchem.2016.07.014_bib34) 2012; 51 Benedek (10.1016/j.jorganchem.2016.07.014_bib25) 2015; 5 Alvarez-Rodriguez (10.1016/j.jorganchem.2016.07.014_bib16) 2015; 300 Metsänen (10.1016/j.jorganchem.2016.07.014_bib10) 2015; 6 Waterman (10.1016/j.jorganchem.2016.07.014_bib14) 2007; 40 Gallego (10.1016/j.jorganchem.2016.07.014_bib38) 2014; 33 Nelson (10.1016/j.jorganchem.2016.07.014_bib4) 2013; 42 Schmid (10.1016/j.jorganchem.2016.07.014_bib17) 1977; 16 Blom (10.1016/j.jorganchem.2016.07.014_bib19) 2013; 19 Diez-Gonzalez (10.1016/j.jorganchem.2016.07.014_bib5) 2009; 109 Someya (10.1016/j.jorganchem.2016.07.014_bib12) 2013; 42 Grumbine (10.1016/j.jorganchem.2016.07.014_bib20) 1993; 115 Fortman (10.1016/j.jorganchem.2016.07.014_bib2) 2011; 40 Stoelzel (10.1016/j.jorganchem.2016.07.014_bib28) 2013; 66 Gallego (10.1016/j.jorganchem.2016.07.014_bib35) 2013; 135 Blom (10.1016/j.jorganchem.2016.07.014_bib27) 2013; 135 Hopkinson (10.1016/j.jorganchem.2016.07.014_bib1) 2014; 510 Blom (10.1016/j.jorganchem.2016.07.014_bib11) 2014; 1 Schneider (10.1016/j.jorganchem.2016.07.014_bib13) 2009; 48 Neumann (10.1016/j.jorganchem.2016.07.014_bib21) 2005; 24 Gunanathan (10.1016/j.jorganchem.2016.07.014_bib31) 2014; 114 |
References_xml | – volume: 89 start-page: 823 year: 1977 end-page: 824 ident: bib15 publication-title: Angew. Chem. – volume: 40 start-page: 5151 year: 2011 end-page: 5169 ident: bib2 publication-title: Chem. Soc. Rev. – volume: 132 start-page: 15890 year: 2010 end-page: 15892 ident: bib29 publication-title: J. Am. Chem. Soc. – volume: 24 start-page: 2008 year: 2005 end-page: 2011 ident: bib21 publication-title: Organometallics – volume: 107 start-page: 874 year: 2007 end-page: 922 ident: bib36 publication-title: Chem. Rev. – volume: 47 start-page: 3122 year: 2008 end-page: 3172 ident: bib3 publication-title: Angew. Chem. Int. Ed. – volume: 111 start-page: 1761 year: 2011 end-page: 1779 ident: bib32 publication-title: Chem. Rev. – volume: 33 start-page: 6885 year: 2014 end-page: 6897 ident: bib38 publication-title: Organometallics – volume: 510 start-page: 485 year: 2014 end-page: 496 ident: bib1 publication-title: Nature – volume: 115 start-page: 7884 year: 1993 end-page: 7885 ident: bib20 publication-title: J. Am. Chem. Soc. – volume: 5 start-page: 5077 year: 2015 end-page: 5086 ident: bib25 publication-title: Rsc Adv. – volume: 300 start-page: 1 year: 2015 end-page: 28 ident: bib16 publication-title: Coord. Chem. Rev. – volume: 128 start-page: 9628 year: 2006 end-page: 9629 ident: bib22 publication-title: J. Am. Chem. Soc. – volume: 51 start-page: 6167 year: 2012 end-page: 6171 ident: bib30 publication-title: Angew. Chem. Int. Ed. – volume: 634 start-page: 1755 year: 2008 end-page: 1758 ident: bib26 publication-title: Z. Anorg. Allg. Chem. – volume: 114 start-page: 12024 year: 2014 end-page: 12087 ident: bib31 publication-title: Chem. Rev. – volume: 16 start-page: 785 year: 1977 end-page: 786 ident: bib17 publication-title: Angew. Chem. Int. Ed. Engl. – volume: 37 start-page: 1776 year: 2008 end-page: 1782 ident: bib6 publication-title: Chem. Soc. Rev. – volume: 54 start-page: 2214 year: 2015 end-page: 2218 ident: bib9 publication-title: Angew. Chem. Int. Ed. – volume: 66 start-page: 1163 year: 2013 end-page: 1170 ident: bib28 publication-title: Aust. J. Chem. – volume: 51 start-page: 3691 year: 2012 end-page: 3694 ident: bib33 publication-title: Angew. Chem. Int. Ed. – volume: 40 start-page: 5084 year: 2011 end-page: 5121 ident: bib37 publication-title: Chem. Soc. Rev. – volume: 41 start-page: 7032 year: 2012 end-page: 7060 ident: bib8 publication-title: Chem. Soc. Rev. – volume: 40 start-page: 712 year: 2007 end-page: 719 ident: bib14 publication-title: Acc. Chem. Res. – volume: 132 start-page: 1123 year: 2010 end-page: 1126 ident: bib23 publication-title: J. Am. Chem. Soc. – volume: 51 start-page: 3314 year: 2012 end-page: 3332 ident: bib7 publication-title: Angew. Chem. Int. Ed. – volume: 42 start-page: 286 year: 2013 end-page: 288 ident: bib12 publication-title: Chem. Lett. – volume: 135 start-page: 6703 year: 2013 end-page: 6713 ident: bib27 publication-title: J. Am. Chem. Soc. – volume: 132 start-page: 3038 year: 2010 end-page: 3046 ident: bib24 publication-title: J. Am. Chem. Soc. – volume: 19 start-page: 40 year: 2013 end-page: 62 ident: bib19 publication-title: Chem. Eur. J. – volume: 48 start-page: 1609 year: 2009 end-page: 1613 ident: bib13 publication-title: Angew. Chem. Int. Ed. – start-page: 2372 year: 2001 end-page: 2373 ident: bib18 publication-title: Chem. Commun. – volume: 135 start-page: 15617 year: 2013 end-page: 15626 ident: bib35 publication-title: J. Am. Chem. Soc. – volume: 42 start-page: 6723 year: 2013 end-page: 6753 ident: bib4 publication-title: Chem. Soc. Rev. – volume: 1 start-page: 134 year: 2014 end-page: 148 ident: bib11 publication-title: Inorg. Chem. Front. – volume: 51 start-page: 11478 year: 2012 end-page: 11482 ident: bib34 publication-title: Angew. Chem. Int. Ed. – volume: 109 start-page: 3612 year: 2009 end-page: 3676 ident: bib5 publication-title: Chem. Rev. – volume: 6 start-page: 7143 year: 2015 end-page: 7149 ident: bib10 publication-title: Chem. Sci. – volume: 48 start-page: 1609 year: 2009 ident: 10.1016/j.jorganchem.2016.07.014_bib13 publication-title: Angew. Chem. Int. Ed. doi: 10.1002/anie.200804993 – volume: 111 start-page: 1761 year: 2011 ident: 10.1016/j.jorganchem.2016.07.014_bib32 publication-title: Chem. Rev. doi: 10.1021/cr1003503 – volume: 51 start-page: 3691 year: 2012 ident: 10.1016/j.jorganchem.2016.07.014_bib33 publication-title: Angew. Chem. Int. Ed. doi: 10.1002/anie.201200632 – volume: 42 start-page: 6723 year: 2013 ident: 10.1016/j.jorganchem.2016.07.014_bib4 publication-title: Chem. Soc. Rev. doi: 10.1039/c3cs60146c – volume: 5 start-page: 5077 year: 2015 ident: 10.1016/j.jorganchem.2016.07.014_bib25 publication-title: Rsc Adv. doi: 10.1039/C4RA14417A – volume: 132 start-page: 3038 year: 2010 ident: 10.1016/j.jorganchem.2016.07.014_bib24 publication-title: J. Am. Chem. Soc. doi: 10.1021/ja910305p – volume: 114 start-page: 12024 year: 2014 ident: 10.1016/j.jorganchem.2016.07.014_bib31 publication-title: Chem. Rev. doi: 10.1021/cr5002782 – volume: 128 start-page: 9628 year: 2006 ident: 10.1016/j.jorganchem.2016.07.014_bib22 publication-title: J. Am. Chem. Soc. doi: 10.1021/ja062928i – volume: 42 start-page: 286 year: 2013 ident: 10.1016/j.jorganchem.2016.07.014_bib12 publication-title: Chem. Lett. doi: 10.1246/cl.2013.286 – volume: 300 start-page: 1 year: 2015 ident: 10.1016/j.jorganchem.2016.07.014_bib16 publication-title: Coord. Chem. Rev. doi: 10.1016/j.ccr.2015.04.008 – volume: 132 start-page: 15890 year: 2010 ident: 10.1016/j.jorganchem.2016.07.014_bib29 publication-title: J. Am. Chem. Soc. doi: 10.1021/ja106458p – volume: 89 start-page: 823 year: 1977 ident: 10.1016/j.jorganchem.2016.07.014_bib15 publication-title: Angew. Chem. doi: 10.1002/ange.19770891116 – volume: 634 start-page: 1755 year: 2008 ident: 10.1016/j.jorganchem.2016.07.014_bib26 publication-title: Z. Anorg. Allg. Chem. doi: 10.1002/zaac.200800131 – volume: 135 start-page: 6703 year: 2013 ident: 10.1016/j.jorganchem.2016.07.014_bib27 publication-title: J. Am. Chem. Soc. doi: 10.1021/ja402480v – volume: 51 start-page: 3314 year: 2012 ident: 10.1016/j.jorganchem.2016.07.014_bib7 publication-title: Angew. Chem. Int. Ed. doi: 10.1002/anie.201106131 – volume: 6 start-page: 7143 year: 2015 ident: 10.1016/j.jorganchem.2016.07.014_bib10 publication-title: Chem. Sci. doi: 10.1039/C5SC02855H – volume: 16 start-page: 785 year: 1977 ident: 10.1016/j.jorganchem.2016.07.014_bib17 publication-title: Angew. Chem. Int. Ed. Engl. doi: 10.1002/anie.197707851 – volume: 54 start-page: 2214 year: 2015 ident: 10.1016/j.jorganchem.2016.07.014_bib9 publication-title: Angew. Chem. Int. Ed. doi: 10.1002/anie.201409739 – volume: 24 start-page: 2008 year: 2005 ident: 10.1016/j.jorganchem.2016.07.014_bib21 publication-title: Organometallics doi: 10.1021/om050010e – volume: 40 start-page: 5084 year: 2011 ident: 10.1016/j.jorganchem.2016.07.014_bib37 publication-title: Chem. Soc. Rev. doi: 10.1039/c1cs15071e – volume: 51 start-page: 11478 year: 2012 ident: 10.1016/j.jorganchem.2016.07.014_bib34 publication-title: Angew. Chem. Int. Ed. doi: 10.1002/anie.201205570 – volume: 132 start-page: 1123 year: 2010 ident: 10.1016/j.jorganchem.2016.07.014_bib23 publication-title: J. Am. Chem. Soc. doi: 10.1021/ja9091374 – volume: 33 start-page: 6885 year: 2014 ident: 10.1016/j.jorganchem.2016.07.014_bib38 publication-title: Organometallics doi: 10.1021/om500966t – volume: 47 start-page: 3122 year: 2008 ident: 10.1016/j.jorganchem.2016.07.014_bib3 publication-title: Angew. Chem. Int. Ed. doi: 10.1002/anie.200703883 – volume: 40 start-page: 5151 year: 2011 ident: 10.1016/j.jorganchem.2016.07.014_bib2 publication-title: Chem. Soc. Rev. doi: 10.1039/c1cs15088j – volume: 41 start-page: 7032 year: 2012 ident: 10.1016/j.jorganchem.2016.07.014_bib8 publication-title: Chem. Soc. Rev. doi: 10.1039/c2cs35102a – volume: 115 start-page: 7884 year: 1993 ident: 10.1016/j.jorganchem.2016.07.014_bib20 publication-title: J. Am. Chem. Soc. doi: 10.1021/ja00070a047 – volume: 51 start-page: 6167 year: 2012 ident: 10.1016/j.jorganchem.2016.07.014_bib30 publication-title: Angew. Chem. Int. Ed. doi: 10.1002/anie.201202175 – volume: 40 start-page: 712 year: 2007 ident: 10.1016/j.jorganchem.2016.07.014_bib14 publication-title: Acc. Chem. Res. doi: 10.1021/ar700028b – volume: 135 start-page: 15617 year: 2013 ident: 10.1016/j.jorganchem.2016.07.014_bib35 publication-title: J. Am. Chem. Soc. doi: 10.1021/ja408137t – volume: 19 start-page: 40 year: 2013 ident: 10.1016/j.jorganchem.2016.07.014_bib19 publication-title: Chem. Eur. J. doi: 10.1002/chem.201203072 – volume: 1 start-page: 134 year: 2014 ident: 10.1016/j.jorganchem.2016.07.014_bib11 publication-title: Inorg. Chem. Front. doi: 10.1039/C3QI00079F – start-page: 2372 year: 2001 ident: 10.1016/j.jorganchem.2016.07.014_bib18 publication-title: Chem. Commun. doi: 10.1039/b108132b – volume: 37 start-page: 1776 year: 2008 ident: 10.1016/j.jorganchem.2016.07.014_bib6 publication-title: Chem. Soc. Rev. doi: 10.1039/b711132k – volume: 66 start-page: 1163 year: 2013 ident: 10.1016/j.jorganchem.2016.07.014_bib28 publication-title: Aust. J. Chem. doi: 10.1071/CH13196 – volume: 107 start-page: 874 year: 2007 ident: 10.1016/j.jorganchem.2016.07.014_bib36 publication-title: Chem. Rev. doi: 10.1021/cr050992x – volume: 109 start-page: 3612 year: 2009 ident: 10.1016/j.jorganchem.2016.07.014_bib5 publication-title: Chem. Rev. doi: 10.1021/cr900074m – volume: 510 start-page: 485 year: 2014 ident: 10.1016/j.jorganchem.2016.07.014_bib1 publication-title: Nature doi: 10.1038/nature13384 |
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Snippet | The present review highlights the role of N-heterocyclic silylene (NHSi) ligands, the silicon analogues of N-heterocyclic carbenes (NHCs), utilized in various... |
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SubjectTerms | Homogeneous catalysis Hydrosilylation Pincer ligands Silicon analogues of carbenes Silylenes |
Title | N-heterocyclic silylenes as powerful steering ligands in catalysis |
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