Size Effect in Hydrogenation of Nitroaromatics Using Support-Immobilized Atomically Precise Gold Clusters

2021 ◽  
Vol 125 (6) ◽  
pp. 3327-3336
Author(s):  
Sam Nesbitt ◽  
Matthew Watson ◽  
Vladimir B. Golovko
Keyword(s):  
Size Effect ◽  
Gold Clusters

Size Effect of Silica-supported Gold Clusters in the Microwave-assisted Oxidation of Benzyl Alcohol with H2O2

2010 ◽  
Vol 39 (3) ◽  
pp. 159-161 ◽  
Author(s):  
Yongmei Liu ◽  
Hironori Tsunoyama ◽  
Tomoki Akita ◽  
Tatsuya Tsukuda
Keyword(s):  
Size Effect ◽  
Benzyl Alcohol ◽  
Gold Clusters ◽  
Microwave Assisted ◽  
Oxidation Of Benzyl Alcohol ◽  
Supported Gold

Optical Limitation induced by Gold Clusters. 1. Size Effect

2000 ◽  
Vol 104 (26) ◽  
pp. 6133-6137 ◽  
Author(s):  
Lionel François ◽  
Mehran Mostafavi ◽  
Jacqueline Belloni ◽  
Jean-François Delouis ◽  
Jacques Delaire ◽  
...  
Keyword(s):  
Size Effect ◽  
Gold Clusters ◽  
Optical Limitation

Size effect on the catalysis of gold clusters dispersed in water for aerobic oxidation of alcohol

2006 ◽  
Vol 429 (4-6) ◽  
pp. 528-532 ◽  
Author(s):  
Hironori Tsunoyama ◽  
Hidehiro Sakurai ◽  
Tatsuya Tsukuda
Keyword(s):  
Size Effect ◽  
Aerobic Oxidation ◽  
Gold Clusters

Quantum-size-effect accommodation of gold clusters with altered fluorescence of dyes

RSC Advances ◽  
2015 ◽  
Vol 5 (39) ◽  
pp. 30610-30616 ◽  
Author(s):  
Xianhu Liu ◽  
Yishi Wu ◽  
Shuanghao Li ◽  
Yan Zhao ◽  
Chengqian Yuan ◽  
...  
Keyword(s):  
Fluorescence Quenching ◽  
Size Effect ◽  
Quantum Size Effect ◽  
Gold Clusters ◽  
Quantum Size

Quantum-size-effect accommodation towards Au25 nanoclusters is demonstrated with tunable fluorescence quenching and enhancement of analyte dyes.

Size Effect of Atomic Gold Clusters for Carbon Monoxide Passivation at Rucore–Ptshell Nanocatalysts

2016 ◽  
Vol 120 (14) ◽  
pp. 7621-7628 ◽  
Author(s):  
Tsan-Yao Chen ◽  
Yu-Ting Liu ◽  
Jeng Han Wang ◽  
Guo-Wei Lee ◽  
Po-Wei Yang ◽  
...  
Keyword(s):  
Carbon Monoxide ◽  
Size Effect ◽  
Gold Clusters

Crystal structure images of large gold clusters and growing crystals by HRTEM

1984 ◽  
Vol 42 ◽  
pp. 428-429
Author(s):  
L.R. Wallenberg ◽  
J.-O. Bovin ◽  
G. Schmid
Keyword(s):  
Crystal Structure ◽  
Nucleation And Growth ◽  
Close Packing ◽  
Gold Clusters ◽  
Molecular Weight Determination ◽  
Growth Mechanisms ◽  
Starting Point ◽  
Different Types ◽  
Nucleation And Growth Mechanisms ◽  
Points Of View

Metallic clusters are interesting from various points of view, e.g. as a mean of spreading expensive catalysts on a support, or following heterogeneous and homogeneous catalytic events. It is also possible to study nucleation and growth mechanisms for crystals with the cluster as known starting point.Gold-clusters containing 55 atoms were manufactured by reducing (C6H5)3PAuCl with B2H6 in benzene. The chemical composition was found to be Au9.2[P(C6H5)3]2Cl. Molecular-weight determination by means of an ultracentrifuge gave the formula Au55[P(C6H5)3]Cl6 A model was proposed from Mössbauer spectra by Schmid et al. with cubic close-packing of the 55 gold atoms in a cubeoctahedron as shown in Fig 1. The cluster is almost completely isolated from the surroundings by the twelve triphenylphosphane groups situated in each corner, and the chlorine atoms on the centre of the 3x3 square surfaces. This gives four groups of gold atoms, depending on the different types of surrounding.

Aldehyde gold clusters for molecular labeling

1995 ◽  
Vol 53 ◽  
pp. 858-859
Author(s):  
James F. Hainfeld ◽  
Frederic R. Furuya
Keyword(s):  
Covalent Bond ◽  
Aldehyde Group ◽  
Gold Clusters ◽  
Side Reactions ◽  
Amino Groups ◽  
Sodium Cyanoborohydride ◽  
Schiff’S Base ◽  
Protein Molecules ◽  
Hydroxysuccinimide Esters ◽  
Primary Amino

Glutaraldehyde is a useful tissue and molecular fixing reagents. The aldehyde moiety reacts mainly with primary amino groups to form a Schiff's base, which is reversible but reasonably stable at pH 7; a stable covalent bond may be formed by reduction with, e.g., sodium cyanoborohydride (Fig. 1). The bifunctional glutaraldehyde, (CHO-(CH2)3-CHO), successfully stabilizes protein molecules due to generally plentiful amines on their surface; bovine serum albumin has 60; 59 lysines + 1 α-amino. With some enzymes, catalytic activity after fixing is preserved; with respect to antigens, glutaraldehyde treatment can compromise their recognition by antibodies in some cases. Complicating the chemistry somewhat are the reported side reactions, where glutaraldehyde reacts with other amino acid side chains, cysteine, histidine, and tyrosine. It has also been reported that glutaraldehyde can polymerize in aqueous solution. Newer crosslinkers have been found that are more specific for the amino group, such as the N-hydroxysuccinimide esters, and are commonly preferred for forming conjugates. However, most of these linkers hydrolyze in solution, so that the activity is lost over several hours, whereas the aldehyde group is stable in solution, and may have an advantage of overall efficiency.

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