Chemoselective Hydrogenation of Benzoic Acid over Ni–Zr–B–PEG(800) Nanoscale Amorphous Alloy in Water

2013 ◽  
Vol 52 (6) ◽  
pp. 2266-2272 ◽  
Author(s):  
Guoyi Bai ◽  
Xin Wen ◽  
Zhen Zhao ◽  
Fei Li ◽  
Huixian Dong ◽  
...  
Keyword(s):  
Amorphous Alloy ◽  
Benzoic Acid ◽  
Chemoselective Hydrogenation

scholarly journals Correction to “Chemoselective Hydrogenation of Benzoic Acid over Ni–Zr–B–PEG(800) Nanoscale Amorphous Alloy in Water”

2015 ◽  
Vol 54 (16) ◽  
pp. 4681-4682 ◽  
Author(s):  
Guoyi Bai ◽  
Xin Wen ◽  
Zhen Zhao ◽  
Fei Li ◽  
Huixian Dong ◽  
...  
Keyword(s):  
Amorphous Alloy ◽  
Benzoic Acid ◽  
Chemoselective Hydrogenation

Significant effect of base on the improvement of selectivity in the hydrogenation of benzoic acid over NiZrB amorphous alloy supported on γ-Al2O3

2015 ◽  
Vol 5 (6) ◽  
pp. 3281-3287 ◽  
Author(s):  
Xin Wen ◽  
Yingying Cao ◽  
Xianliang Qiao ◽  
Libo Niu ◽  
Li Huo ◽  
...  
Keyword(s):  
Amorphous Alloy ◽  
Benzoic Acid ◽  
Cyclohexanecarboxylic Acid

The selectivity for cyclohexanecarboxylic acid was significantly enhanced by adding small amounts of bases in benzoic acid hydrogenation.

ChemInform Abstract: A NiPdB-PEG(800) Amorphous Alloy Catalyst for the Chemoselective Hydrogenation of Electron-Deficient Aromatic Substrates.

ChemInform ◽  
2014 ◽  
Vol 45 (31) ◽  
pp. no-no
Author(s):  
Guoyi Bai ◽  
Zhen Zhao ◽  
Huixian Dong ◽  
Libo Niu ◽  
Yalong Wang ◽  
...  
Keyword(s):  
Amorphous Alloy ◽  
Aromatic Substrates ◽  
Chemoselective Hydrogenation ◽  
Alloy Catalyst

A NiPdB-PEG(800) Amorphous Alloy Catalyst for the Chemoselective Hydrogenation of Electron-Deficient Aromatic Substrates

ChemCatChem ◽  
2013 ◽  
Vol 6 (2) ◽  
pp. 655-662 ◽  
Author(s):  
Guoyi Bai ◽  
Zhen Zhao ◽  
Huixian Dong ◽  
Libo Niu ◽  
Yalong Wang ◽  
...  
Keyword(s):  
Amorphous Alloy ◽  
Aromatic Substrates ◽  
Chemoselective Hydrogenation ◽  
Alloy Catalyst

scholarly journals Corrigendum: A NiPdB-PEG(800) Amorphous Alloy Catalyst for the Chemoselective Hydrogenation of Electron-Deficient Aromatic Substrates

ChemCatChem ◽  
2015 ◽  
Vol 7 (16) ◽  
pp. 2407-2407
Author(s):  
Guoyi Bai ◽  
Zhen Zhao ◽  
Huixian Dong ◽  
Libo Niu ◽  
Yalong Wang ◽  
...  
Keyword(s):  
Amorphous Alloy ◽  
Aromatic Substrates ◽  
Chemoselective Hydrogenation ◽  
Alloy Catalyst

Efficient hydrogenation of aromatic aldehydes to corresponding benzyl alcohols over Ni–B/MIL-101

RSC Advances ◽  
2014 ◽  
Vol 4 (63) ◽  
pp. 33564-33568 ◽  
Author(s):  
Xiangjin Kong ◽  
Junhai Liu
Keyword(s):  
Liquid Phase ◽  
Amorphous Alloy ◽  
Aromatic Aldehydes ◽  
Impregnation Method ◽  
Benzyl Alcohols ◽  
Catalytic Activities ◽  
Chemoselective Hydrogenation ◽  
Alloy Particles ◽  
Simple Reduction

Ni–B amorphous alloy particles incorporated onto MIL-101 were prepared by a simple reduction impregnation method, and exhibited excellent catalytic activities for liquid-phase chemoselective hydrogenation of aromatic aldehydes to corresponding benzyl alcohols.

TEM characterization of proton-exchanged LiNbO3 optical waveguides

1986 ◽  
Vol 44 ◽  
pp. 480-481
Author(s):  
W. E. Lee
Keyword(s):  
Refractive Index ◽  
Benzoic Acid ◽  
Optical Waveguides ◽  
Total Internal Reflection ◽  
Index Of Refraction ◽  
Optical Measurements ◽  
Lithium Ions ◽  
Wide Channel ◽  
Tem Characterization

An optical waveguide consists of a several-micron wide channel with a slightly different index of refraction than the host substrate; light can be trapped in the channel by total internal reflection.Optical waveguides can be formed from single-crystal LiNbO3 using the proton exhange technique. In this technique, polished specimens are masked with polycrystal1ine chromium in such a way as to leave 3-13 μm wide channels. These are held in benzoic acid at 249°C for 5 minutes allowing protons to exchange for lithium ions within the channels causing an increase in the refractive index of the channel and creating the waveguide. Unfortunately, optical measurements often reveal a loss in waveguiding ability up to several weeks after exchange.

Bjerkandera adusta as a source of benzoic acid derivatives targeting 26S proteasome and cathepsins B&L

2019 ◽  
Author(s):  
K Georgousaki ◽  
N Tsafantakis ◽  
S Gumeni ◽  
V González-Menéndez ◽  
G Lambrinidis ◽  
...  
Keyword(s):  
Benzoic Acid ◽  
26S Proteasome ◽  
Bjerkandera Adusta ◽  
Benzoic Acid Derivatives
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