scholarly journals Divergent Pathways Involving 1,3-Dipolar Addition and N−N Bond Splitting of an Organic Azide across a Zirconium Methylidene

2018 ◽  
Vol 130 (7) ◽  
pp. 1996-1999 ◽  
Author(s):  
Takashi Kurogi ◽  
Manoj V. Mane ◽  
Shuai Zheng ◽  
Patrick J. Carroll ◽  
Mu-Hyun Baik ◽  
...  
Keyword(s):  
Organic Azide ◽  
Bond Splitting

scholarly journals Divergent Pathways Involving 1,3-Dipolar Addition and N−N Bond Splitting of an Organic Azide across a Zirconium Methylidene

2018 ◽  
Vol 57 (7) ◽  
pp. 1978-1981 ◽  
Author(s):  
Takashi Kurogi ◽  
Manoj V. Mane ◽  
Shuai Zheng ◽  
Patrick J. Carroll ◽  
Mu-Hyun Baik ◽  
...  
Keyword(s):  
Organic Azide ◽  
Bond Splitting

Carbon nanodots, Ru nanodots and hybrid nanodots: preparation and catalytic properties

2015 ◽  
Vol 3 (29) ◽  
pp. 15074-15081 ◽  
Author(s):  
Abhijit Biswas ◽  
Subir Paul ◽  
Arindam Banerjee
Keyword(s):  
Catalytic Activity ◽  
Functional Groups ◽  
Catalytic Properties ◽  
Carbon Nanodots ◽  
Organic Azide

Peptide functionalized carbon nanodot supported Ru nanodots have been synthesized, which show a remarkable and reusable catalytic activity for the transformation of organic azide to the corresponding amine in the presence of other functional groups in water.

scholarly journals STUDY ON THE BOND SPLITTING STRENGTH OF SHEATHS FOR A PRECAST CONCRETE SYSTEM

1995 ◽  
Vol 60 (473) ◽  
pp. 137-148
Author(s):  
Rodolfo YANEZ ◽  
Juan Jose CASTRO ◽  
Teruaki YAMAGUCHI ◽  
Hiroshi IMAI
Keyword(s):  
Precast Concrete ◽  
Concrete System ◽  
Splitting Strength ◽  
Bond Splitting

P−C Bond Splitting Reactions in Ruthenium(II) Complexes of Binap and MeO−Biphep Using CF3SO3H and HBF4. A Novel Ru−F−H Interaction

2000 ◽  
Vol 19 (3) ◽  
pp. 309-316 ◽  
Author(s):  
Carolien J. den Reijer ◽  
Michael Wörle ◽  
Paul S. Pregosin
Keyword(s):  
Bond Splitting

scholarly journals Organic Azide Inhibitors of Cysteine Proteases [J.Am. Chem. Soc.2006,128, 12396−12397].

2007 ◽  
Vol 129 (30) ◽  
pp. 9532-9532
Author(s):  
Giang Thanh Le ◽  
Giovanni Abbenante ◽  
Praveen K. Madala ◽  
Huy N. Hoang ◽  
David P. Fairlie
Keyword(s):  
Cysteine Proteases ◽  
Organic Azide

Hydrogenation of cinnamyl methyl ether and allylbenzene on palladium catalysts

1987 ◽  
Vol 52 (4) ◽  
pp. 1015-1020 ◽  
Author(s):  
Libor Červený ◽  
Ivo Paseka ◽  
Eva Fialová ◽  
Vlastimil Růžička
Keyword(s):  
Double Bond ◽  
Solvent Effect ◽  
Benzene Ring ◽  
Methyl Ether ◽  
Atmospheric Pressure ◽  
Palladium Catalysts ◽  
Polar Medium ◽  
Adsorbed Molecules ◽  
Ionic Nature ◽  
Bond Splitting

The hydrogenation of cinnamyl methyl ether and allylbenzene in hexane and acetone at 20 °C and atmospheric pressure of hydrogen has been studied on eight palladium catalysts. The hydrogenation of cinnamyl methyl ether is accompanied by C-O bond splitting giving rise to propylbenzene and methanol, the hydrogenation of allylbenzene is associated with the isomerization of the double bond resulting in its conjugation with the benzene ring. A marked solvent effect on the selectivity of hydrogenation of cinnamyl methyl ether has been observed and ascribed to the effect of solvated protons on the adsorbed molecules of the ether which is promoted by polar medium. The solvent effect on the isomerization of allylbenzene during the hydrogenation is little pronounced, which suggests that this reaction is not of ionic nature.

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