scholarly journals Recent advances in the development of alkyne metathesis catalysts

2011 ◽  
Vol 7 ◽  
pp. 82-93 ◽  
Author(s):  
Xian Wu ◽  
Matthias Tamm
Keyword(s):  
Alkyne Metathesis ◽  
Highly Active ◽  
Recent Advances ◽  
Metathesis Reactions ◽  
Metathesis Catalysts ◽  
And Tungsten

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.

scholarly journals Efficient catalytic alkyne metathesis with a fluoroalkoxy-supported ditungsten(III) complex

2018 ◽  
Vol 14 ◽  
pp. 2425-2434 ◽  
Author(s):  
Henrike Ehrhorn ◽  
Janin Schlösser ◽  
Dirk Bockfeld ◽  
Matthias Tamm
Keyword(s):  
Metal Complexes ◽  
The Self ◽  
Significant Activity ◽  
Terminal Alkynes ◽  
Alkyne Metathesis ◽  
Cross Metathesis ◽  
Tungsten Complexes ◽  
Highly Active ◽  
Metathesis Catalysts ◽  
And Tungsten

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.

Preparation of Imidazolin-2-iminato Molybdenum and Tungsten Benzylidyne Complexes: A New Pathway to Highly Active Alkyne Metathesis Catalysts

2010 ◽  
Vol 16 (29) ◽  
pp. 8868-8877 ◽  
Author(s):  
Birte Haberlag ◽  
Xian Wu ◽  
Kai Brandhorst ◽  
Jörg Grunenberg ◽  
Constantin G. Daniliuc ◽  
...  
Keyword(s):  
Alkyne Metathesis ◽  
Highly Active ◽  
Metathesis Catalysts ◽  
And Tungsten

Arylene–ethynylene macrocycles: Privileged shape-persistent building blocks for organic materials

2012 ◽  
Vol 84 (4) ◽  
pp. 869-878 ◽  
Author(s):  
Dustin E. Gross ◽  
Ling Zang ◽  
Jeffrey S. Moore
Keyword(s):  
Functional Group ◽  
Organic Materials ◽  
Building Blocks ◽  
Alkyne Metathesis ◽  
Reaction Conditions ◽  
Traditional Methods ◽  
Dynamic Covalent Chemistry ◽  
Highly Active ◽  
Recent Advances ◽  
Metathesis Catalyst

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.

scholarly journals Highly active alkyne metathesis catalysts operating under open air condition

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Yanqing Ge ◽  
Shaofeng Huang ◽  
Yiming Hu ◽  
Lei Zhang ◽  
Ling He ◽  
...  
Keyword(s):  
Catalyst System ◽  
Alkyne Metathesis ◽  
Ambient Conditions ◽  
High Moisture ◽  
Highly Active ◽  
Active User ◽  
Metathesis Catalyst ◽  
Cyano Groups ◽  
Metathesis Catalysts ◽  
User Friendly

AbstractAlkyne metathesis represents a rapidly emerging synthetic method that has shown great potential in small molecule and polymer synthesis. However, its practical use has been impeded by the limited availability of user-friendly catalysts and their generally high moisture/air sensitivity. Herein, we report an alkyne metathesis catalyst system that can operate under open-air conditions with a broad substrate scope and excellent yields. These catalysts are composed of simple multidentate tris(2-hydroxyphenyl)methane ligands, which can be easily prepared in multi-gram scale. The catalyst substituted with electron withdrawing cyano groups exhibits the highest activity at room temperature with excellent functional group tolerance (-OH, -CHO, -NO2, pyridyl). More importantly, the catalyst provides excellent yields (typically >90%) in open air, comparable to those operating under argon. When dispersed in paraffin wax, the active catalyst can be stored on a benchtop under ambient conditions without any decrease in activity for one day (retain 88% after 3 days). This work opens many possibilities for developing highly active user-friendly alkyne metathesis catalysts that can function in open air.

ChemInform Abstract: Highly Active Multidentate Ligand-Based Alkyne Metathesis Catalysts.

ChemInform ◽  
2016 ◽  
Vol 47 (43) ◽  
Author(s):  
Ya Du ◽  
Haishen Yang ◽  
Chengpu Zhu ◽  
Michael Ortiz ◽  
Kenji D. Okochi ◽  
...  
Keyword(s):  
Alkyne Metathesis ◽  
Multidentate Ligand ◽  
Highly Active ◽  
Metathesis Catalysts
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