Faceted Colloidal Metallic Ni3N Nanocrystals: Size-Controlled Solution-Phase Synthesis and Electrochemical Overall Water Splitting

2021 ◽  
Vol 4 (3) ◽  
pp. 2165-2173
Author(s):  
G. Shiva Shanker ◽  
Satishchandra Ogale
2014 ◽  
Vol 50 (79) ◽  
pp. 11753-11756 ◽  
Author(s):  
Cuiling Li ◽  
Takaaki Sato ◽  
Yusuke Yamauchi

We report a solution phase synthesis of monodispersed mesoporous Pd nanoparticles (MPNs) with narrow particle size distributions.


Author(s):  
Abinaya Annamalai ◽  
Dipak Vijaykumar Shinde ◽  
Joka Buha ◽  
Sergio Marras ◽  
Mirko Prato ◽  
...  

Hollow structures made of nanoscale building blocks are of great interest as catalysts for electrochemical water splitting. Here we report a solution-phase synthesis of yolk-shell Co3O4/Co1-xRuxO2 microspheres (MSs) having a...


Author(s):  
François Morvan ◽  
Aude-Emmanuelle Navarro ◽  
Cécile Dueymes ◽  
Ilaria Adamo ◽  
Andreas Schoenberger ◽  
...  

ChemInform ◽  
2010 ◽  
Vol 33 (35) ◽  
pp. 123-123
Author(s):  
Young K. Yun ◽  
John A. Porco Jr. ◽  
Jeff Labadie

1995 ◽  
Vol 5 (1) ◽  
pp. 39-47 ◽  
Author(s):  
ISABELLE BARBER ◽  
JEAN-LOUIS IMBACH ◽  
BERNARD RAYNER

2003 ◽  
Vol 6 (2) ◽  
pp. 181-184 ◽  
Author(s):  
Changhua An ◽  
Kaibin Tang ◽  
Bin Hai ◽  
Guozhen Shen ◽  
Chunrui Wang ◽  
...  

2009 ◽  
Vol 36 (4) ◽  
pp. 362-373 ◽  
Author(s):  
CHU-BIAO XUE ◽  
ARIEL EWENSON ◽  
JEFFREY M. BECKER ◽  
FRED NAIDER

1989 ◽  
Vol 42 (9) ◽  
pp. 1519 ◽  
Author(s):  
RM Valerio ◽  
JW Perich ◽  
EA Kitas ◽  
PF Alewood ◽  
RB Johns

The PTyr (O-phosphotyrosine) pentapeptide H-Asn-Glu-Tyr(PO3H2)-Thr-Ala-OH.HO2CCF3, which is a naturally occurring sequence from the autophosphorylated Rous sarcoma virus pp60V-SrC, was prepared in high yield by the use of Boc-Tyr(PO3Me2)-OH in the Boc mode of solution-phase peptide synthesis. The protected pentapeptide, Z-Asn-Glu(OBzl)-Tyr(PO3Me2)-Thr(Bzl)-Ala-OBzl, was deprotected by a two-stage procedure which involved initial palladium-catalysed hydrogenolysis followed by the removal of the phosphate methyl groups by the use of one of the following treatments: (A) 10% bromotrimethylsilane/acetonitrile, (B) 1 M bromotrimethylsilane/thioanisole in trifluoroacetic acid, or (C) trifluoromethanesulfonic acid/trifluoroacetic acid/dimethyl sulfide/m-cresol.


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