Csp3−H Activation without Chelation Assistance in an Iridium Pincer Complex Forming Cyclometallated Products

2017 ◽  
Vol 23 (8) ◽  
pp. 1748-1751 ◽  
Author(s):  
David A. Ahlstrand ◽  
Alexey V. Polukeev ◽  
Rocío Marcos ◽  
Mårten S. G. Ahlquist ◽  
Ola F. Wendt
Keyword(s):  
2021 ◽  
Author(s):  
Nicholas Wiedmaier ◽  
Hartmut Schubert ◽  
Hermann A Mayer ◽  
Lars Wesemann

The ruthenium carbene pincer complex 2 was synthesized treating the benzo annulated cycloheptatriene bisphosphine 1 with RuCl3. Addition of three equivalents of hydrogen to the carbocyclic carbene complex 2 was...


2016 ◽  
Vol 358 (20) ◽  
pp. 3283-3292 ◽  
Author(s):  
Nerea Conde ◽  
Raul SanMartin ◽  
María Teresa Herrero ◽  
Esther Domínguez

2009 ◽  
pp. 3270 ◽  
Author(s):  
Kenneth J. H. Young ◽  
Jonas Oxgaard ◽  
Daniel H. Ess ◽  
Steven K. Meier ◽  
Timothy Stewart ◽  
...  

2021 ◽  
Author(s):  
Quinton Bruch ◽  
Santanu Malakar ◽  
Alan Goldman ◽  
Alexander Miller

Molybdenum complexes supported by tridentate pincer ligands are exceptional catalysts for dinitrogen fixation using chemical reductants, but little is known about their prospects for electrochemical reduction of dinitrogen. The viability of electrochemical N2 binding and splitting by a molybdenum(III) pincer complex, (pyPNP)MoBr3 (pyPNP = 2,6-bis(tBu2PCH2)-C5H3N)), is established in this work, providing a foundation for a detailed mechanistic study of electrode-driven formation of the nitride complex (pyPNP)Mo(N)Br. Electrochemical kinetic analysis, optical and vibrational spectroelectrochemical monitoring, and computational studies point to two reaction pathways: in the “reaction layer” pathway, the molybdenum(III) precursor is reduced by 2e– and generates a bimetallic molybdenum(I) Mo2(-N2) species capable of N–N bond scission. In the “bulk solution” pathway the precursor is reduced by 3e– at the electrode surface to generate molybdenum(0) species that undergo chemical redox reactions via comproportionation in the bulk solution away from the electrode surface to generate the same bimetallic molybdenum(I) species capable of N2 cleavage. The comproportionation reactions reveal the surprising intermediacy of dimolybdenum(0) complex trans,trans-[(pyPNP)Mo(N2)2](-N2) in N2 splitting pathways. The same “over-reduced” molybdenum(0) species was also found to cleave N2 upon addition of lutidinium, an acid frequently used in catalytic reduction of dinitrogen.


2021 ◽  
Author(s):  
Nana Ma ◽  
Qingli Xu ◽  
Chenhao Tu ◽  
Wenyue Guo ◽  
Guisheng Zhang

It has been reported that either the boryl formate (HCOOBR2), bis(boryl)acetal (R2BOCH2OBR2), or methoxy borane (R2BOCH3) product of CO2 reduction is selectively afforded adopting the Nickel (Ni) pincer catalyst by...


2020 ◽  
Vol 2020 (15-16) ◽  
pp. 1402-1410
Author(s):  
Richt S. van Alten ◽  
Florian Wätjen ◽  
Serhiy Demeshko ◽  
Alexander J. M. Miller ◽  
Christian Würtele ◽  
...  
Keyword(s):  

2012 ◽  
Vol 51 (13) ◽  
pp. 3174-3177 ◽  
Author(s):  
Shoma Anabuki ◽  
Hiroshi Shinokubo ◽  
Naoki Aratani ◽  
Atsuhiro Osuka
Keyword(s):  

2018 ◽  
Vol 57 (44) ◽  
Author(s):  
Felix Schneck ◽  
Florian Schendzielorz ◽  
Nareh Hatami ◽  
Markus Finger ◽  
Christian Würtele ◽  
...  

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