Thermal chemistry of molybdenum complex CpMo(NO)(CH2CMe3)2: Lewis base adducts of CpMo(NO)(:CHCMe3) and a new bonding mode for nitric oxide

1993 ◽  
Vol 12 (9) ◽  
pp. 3575-3585 ◽  
Author(s):  
Peter Legzdins ◽  
Steven J. Rettig ◽  
John E. Veltheer ◽  
Raymond J. Batchelor ◽  
Frederick W. B. Einstein
2016 ◽  
Vol 56 (1) ◽  
pp. 573-582 ◽  
Author(s):  
Diana Fabulyak ◽  
Rex C. Handford ◽  
Aaron S. Holmes ◽  
Taleah M. Levesque ◽  
Russell J. Wakeham ◽  
...  
Keyword(s):  

2014 ◽  
Vol 43 (44) ◽  
pp. 16610-16613 ◽  
Author(s):  
Takako Muraoka ◽  
Keisuke Abe ◽  
Haruhiko Kimura ◽  
Youhei Haga ◽  
Keiji Ueno ◽  
...  

Base-stabilized silanone molybdenum complexes were synthesized by the oxygenation of the MSi bond in the silyl(silylene)molybdenum complex with 1 eq. of PNO in the presence of Lewis base L.


2012 ◽  
Vol 84 (11) ◽  
pp. 2203-2217 ◽  
Author(s):  
Gerhard Erker

The chemistry of some reactive frustrated Lewis pairs (FLPs) is reported. This includes intramolecular P/B and N/B FLPs, some of which were used as catalysts for the hydrogenation of electron-rich olefin substrates. Some advanced intermolecular FLPs are reported, which includes systems derived from very bulky alkenyl boranes obtained from 1,1-carboboration reactions of 1-alkynes with tris(pentafluorophenyl)borane. Some such systems activate dihydrogen and transfer the resulting proton/hydride pair even to some electron-poor alkynes. Eventually, we report on the reaction of our intramolecular ethylene-bridged P/B FLP with nitric oxide (NO). N,B-addition of the P-Lewis base/B-Lewis acid combination is observed to form a new type of a persistent aminoxyl radical. Some of the chemistry of the new FLP-NO radicals is presented and discussed.


Author(s):  
Chi-Ming Wei ◽  
Margarita Bracamonte ◽  
Shi-Wen Jiang ◽  
Richard C. Daly ◽  
Christopher G.A. McGregor ◽  
...  

Nitric oxide (NO) is a potent endothelium-derived relaxing factor which also may modulate cardiomyocyte inotropism and growth via increasing cGMP. While endothelial nitric oxide synthase (eNOS) isoforms have been detected in non-human mammalian tissues, expression and localization of eNOS in the normal and failing human myocardium are poorly defined. Therefore, the present study was designed to investigate eNOS in human cardiac tissues in the presence and absence of congestive heart failure (CHF).Normal and failing atrial tissue were obtained from six cardiac donors and six end-stage heart failure patients undergoing primary cardiac transplantation. ENOS protein expression and localization was investigated utilizing Western blot analysis and immunohistochemical staining with the polyclonal rabbit antibody to eNOS (Transduction Laboratories, Lexington, Kentucky).


2001 ◽  
Vol 28 (5-6) ◽  
pp. 459-462
Author(s):  
Pini Orbach ◽  
Charles E Wood ◽  
Maureen Keller-Wood
Keyword(s):  

2001 ◽  
Vol 120 (5) ◽  
pp. A684-A684
Author(s):  
I DANIELS ◽  
I MURRAY ◽  
W GODDARD ◽  
R LONG

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