scholarly journals Synthesis of Alkyne Metathesis Catalysts from Tris(dimethylamido)tungsten Precursors

2020 ◽  
Vol 2020 (47) ◽  
pp. 4454-4464
Author(s):  
Daniel Melcher ◽  
Òscar Àrias ◽  
Matthias Freytag ◽  
Peter G. Jones ◽  
Matthias Tamm
Author(s):  
Richard R. Thompson ◽  
Madeline E. Rotella ◽  
Xin Zhou ◽  
Frank R. Fronczek ◽  
Osvaldo Gutierrez ◽  
...  

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.


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.


ChemInform ◽  
2013 ◽  
Vol 44 (32) ◽  
pp. no-no
Author(s):  
Haishen Yang ◽  
Zhenning Liu ◽  
Wei Zhang

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