ChemInform Abstract: Recent Advances in the Development of Alkyne Metathesis Catalysts

ChemInform ◽  
2011 ◽  
Vol 42 (36) ◽  
pp. no-no
Author(s):  
Xian Wu ◽  
Matthias Tamm
2011 ◽  
Vol 7 ◽  
pp. 82-93 ◽  
Author(s):  
Xian Wu ◽  
Matthias Tamm

The number of well-defined molybdenum and tungsten alkylidyne complexes that are able to catalyze alkyne metathesis reactions efficiently has been significantly expanded in recent years.The latest developments in this field featuring highly active imidazolin-2-iminato- and silanolate–alkylidyne complexes are outlined in this review.


Author(s):  
Richard R. Thompson ◽  
Madeline E. Rotella ◽  
Xin Zhou ◽  
Frank R. Fronczek ◽  
Osvaldo Gutierrez ◽  
...  

2020 ◽  
Vol 2020 (47) ◽  
pp. 4454-4464
Author(s):  
Daniel Melcher ◽  
Òscar Àrias ◽  
Matthias Freytag ◽  
Peter G. Jones ◽  
Matthias Tamm

1985 ◽  
Vol 28 (1-3) ◽  
pp. 1-8 ◽  
Author(s):  
Richard R. Schrock ◽  
John H. Freudenberger ◽  
Mark L. Listemann ◽  
Laughlin G. McCullough

2012 ◽  
Vol 84 (4) ◽  
pp. 869-878 ◽  
Author(s):  
Dustin E. Gross ◽  
Ling Zang ◽  
Jeffrey S. Moore

This report details the advances in synthetic strategies toward arylene–ethynylene macrocycles (AEMs). After a brief description of traditional methods, we summarize recent advances based on dynamic covalent chemistry (DCC) whereby a highly active and functional group tolerant alkyne metathesis catalyst yields scalable quantities of AEMs under thermodynamic controlled reaction conditions.


2018 ◽  
Vol 14 ◽  
pp. 2425-2434 ◽  
Author(s):  
Henrike Ehrhorn ◽  
Janin Schlösser ◽  
Dirk Bockfeld ◽  
Matthias Tamm

The molybdenum and tungsten complexes M2(OR)6 (Mo2F6, M = Mo, R = C(CF3)2Me; W2F3, M = W, R = OC(CF3)Me2) were synthesized as bimetallic congeners of the highly active alkyne metathesis catalysts [MesC≡M{OC(CF3) n Me3− n }] (MoF6, M = Mo, n = 2; WF3, M = W, n = 1; Mes = 2,4,6-trimethylphenyl). The corresponding benzylidyne complex [PhC≡W{OC(CF3)Me2}] (W Ph F3) was prepared by cleaving the W≡W bond in W2F3 with 1-phenyl-1-propyne. The catalytic alkyne metathesis activity of these metal complexes was determined in the self-metathesis, ring-closing alkyne metathesis and cross-metathesis of internal and terminal alkynes, revealing an almost equally high metathesis activity for the bimetallic tungsten complex W2F3 and the alkylidyne complex W Ph F3. In contrast, Mo2F6 displayed no significant activity in alkyne metathesis.


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