Ultrasmall Pd/Au bimetallic nanocrystals embedded in hydrogen-bonded supramolecular structures: facile synthesis and catalytic activities in the reduction of 4-nitrophenol

2015 ◽  
Vol 3 (38) ◽  
pp. 19433-19438 ◽  
Author(s):  
Feng Jiang ◽  
Ruimin Li ◽  
Jianhua Cai ◽  
Wei Xu ◽  
Anmin Cao ◽  
...  

A hydrogen-bonded supramolecular structure supported with ultrasmall Au, Pd bimetallic nanoparticles was readily synthesized and showed unusual catalytic properties.

Molecules ◽  
2021 ◽  
Vol 26 (15) ◽  
pp. 4528
Author(s):  
Katarína Šuchová ◽  
Vladimír Puchart ◽  
Nikolaj Spodsberg ◽  
Kristian B. R. Mørkeberg Krogh ◽  
Peter Biely

Catalytic properties of GH30 xylanases belonging to subfamilies 7 and 8 were compared on glucuronoxylan, modified glucuronoxylans, arabinoxylan, rhodymenan, and xylotetraose. Most of the tested bacterial GH30-8 enzymes are specific glucuronoxylanases (EC 3.2.1.136) requiring for action the presence of free carboxyl group of MeGlcA side residues. These enzymes were not active on arabinoxylan, rhodymenan and xylotetraose, and conversion of MeGlcA to its methyl ester or its reduction to MeGlc led to a remarkable drop in their specific activity. However, some GH30-8 members are nonspecific xylanases effectively hydrolyzing all tested substrates. In terms of catalytic activities, the GH30-7 subfamily is much more diverse. In addition to specific glucuronoxylanases, the GH30-7 subfamily contains nonspecific endoxylanases and predominantly exo-acting enzymes. The activity of GH30-7 specific glucuronoxylanases also depend on the presence of the MeGlcA carboxyl, but not so strictly as in bacterial enzymes. The modification of the carboxyl group of glucuronoxylan had only weak effect on the action of predominantly exo-acting enzymes, as well as nonspecific xylanases. Rhodymenan and xylotetraose were the best substrates for exo-acting enzymes, while arabinoxylan represented hardly degradable substrate for almost all tested GH30-7 enzymes. The results expand current knowledge on the catalytic properties of this relatively novel group of xylanases.


2009 ◽  
Vol 62 (12) ◽  
pp. 1964-1971 ◽  
Author(s):  
Shengli Huang ◽  
Hongwei Hou ◽  
Liwei Mi ◽  
Yaoting Fan

2021 ◽  
Vol 866 ◽  
pp. 158778
Author(s):  
Yury V. Shubin ◽  
Yury I. Bauman ◽  
Pavel E. Plyusnin ◽  
Ilya V. Mishakov ◽  
Maria S. Tarasenko ◽  
...  

2007 ◽  
Vol 23 (5) ◽  
pp. 508-510
Author(s):  
L SUN ◽  
K WANG ◽  
S LUO ◽  
Q GUO ◽  
C HU

2019 ◽  
Vol 48 (34) ◽  
pp. 12956-12963 ◽  
Author(s):  
Xinyi Ma ◽  
Peipei He ◽  
Baijie Xu ◽  
Jingkun Lu ◽  
Rong Wan ◽  
...  

The catalytic properties and polyanionic structure of pyrazine dicarboxylate-bridged arsenotungstate are reported.


Author(s):  
Andrei S. Batsanov ◽  
Niels Svenstrup ◽  
Jesper Lau ◽  
Jan Becher ◽  
Martin R. Bryce ◽  
...  

2004 ◽  
Vol 357 (12) ◽  
pp. 3746-3752 ◽  
Author(s):  
Igor O. Fritsky ◽  
Jolanta Świątek-Kozłowska ◽  
Agnieszka Dobosz ◽  
Tatiana Yu. Sliva ◽  
Nikolay M. Dudarenko

2003 ◽  
Vol 59 (2) ◽  
pp. 263-276 ◽  
Author(s):  
Manuel Melguizo ◽  
Antonio Quesada ◽  
John N. Low ◽  
Christopher Glidewell

The molecular and supramolecular structures of eight N 4-substituted 2,4-diamino-6-benzyloxy-5-nitrosopyrimidines are discussed, along with one analogue containing no nitroso substituent. The nitroso derivatives all exhibit polarized molecular-electronic structures leading to extensive charge-assisted hydrogen bonding between the molecules. The intermolecular interactions include hard hydrogen bonds of N—H...O and N—H...N types, together with O—H...O and O—H...N types in the monohydrate of 2-amino-6-benzyloxy-4-piperidino-5-nitrosopyrimidine, soft hydrogen bonds of C—H...O, C—H...π(arene) and N—H...π(arene) types and aromatic π...π stacking interactions. The predominant supramolecular structure types take the form of chains and sheets, but no two of the structures determined here exhibit the same combination of hydrogen-bond types.


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