A Pulsed Electron Nuclear Double Resonance Study of the Lewis Acid Site−Nitric Oxide Complex in Zeolite H-ZSM-5

1998 ◽  
Vol 120 (19) ◽  
pp. 4879-4880 ◽  
Author(s):  
Andreas Pöppl ◽  
Thomas Rudolf ◽  
Dieter Michel
Nano Letters ◽  
2021 ◽  
Author(s):  
Shenghua Chen ◽  
Bingqing Wang ◽  
Jiexin Zhu ◽  
Liqiang Wang ◽  
Honghui Ou ◽  
...  

2021 ◽  
Vol 16 ◽  
Author(s):  
Yaser Nejaty Jahromy

Background: Nitric oxide synthase (NOS) catalyzes the formation of nitric oxide (NO) and citrulline from L-arginine, dioxygen (O2), and nicotinamide adenine dinucleotide phosphate (NADPH) in a two-step reaction, with the enzyme-bound intermediate Nω-hydroxy-L-arginine (NHA). Previous electron paramagnetic resonance (EPR) studies of NOS reaction have shown that (6R, 1'R, 2'S)-6-(l',2'-dihydroxypropyl)-5,6,7,8-tetrahydropterin (H4B) acts as a single electron donor in both steps of the reaction, resulting in the transient generation of a tetrahydropterin cation radical (H4B•+). Results: H4B•+ can also be chemically generated in strongly acidic solutions. EPR studies of chemically generated H4B•+ and similar pterin radicals date back to the 1960s. However, the reported paramagnetic parameters of H4B•+ in NOS do not seem to match the corresponding reported parameters for either H4B•+ or other pterin centered radicals chemically generated in solution. In particular, the rather isotropic hyperfine coupling of ca. 45 MHz for 1H6 of H4B•+ in NOS is at least 15 MHz larger than that of H4B•+ or any other previously studies pterin solution radical. In the work reported here, a combination of 9.5 - 9.8 GHz contentious wave (cw-) EPR, 34GHz 1H electron nuclear double resonance (ENDOR), spectral simulation and Density Functional Theory (DFT) calculations were used to investigate this seeming discrepancy. Conclusion: We demonstrated that the differences in the paramagnetic parameters of the chemically generated H4B radicals in solutions and those of the H4B radicals in NOS are consistent with the presence of two different conformers of the same cation radical in the two media.


Small ◽  
2016 ◽  
Vol 12 (17) ◽  
pp. 2334-2343 ◽  
Author(s):  
Ruyi Zou ◽  
Pei-Zhou Li ◽  
Yong-Fei Zeng ◽  
Jia Liu ◽  
Ruo Zhao ◽  
...  

ACS Catalysis ◽  
2018 ◽  
Vol 9 (1) ◽  
pp. 701-715 ◽  
Author(s):  
Taha Salavati-fard ◽  
Efterpi S. Vasiliadou ◽  
Glen R. Jenness ◽  
Raul F. Lobo ◽  
Stavros Caratzoulas ◽  
...  

Author(s):  
Yuanyuan Yue ◽  
Jing Fu ◽  
Chuanming Wang ◽  
Pei Yuan ◽  
Xiaojun Bao ◽  
...  

2019 ◽  
Vol 4 (2) ◽  
pp. 100
Author(s):  
Deasi Adhiani Farida ◽  
Abdulloh Abdulloh ◽  
Ahmadi Jaya Permana

ABSTRACT          Aluminosilicate can be used for cracking reaction. In this study, catalyst of H-aluminosilicate has been synthesized by hydrothermal method with ratio molar Si/Al is 20. The characterizations has been performed by XRD, FTIR and acidity test. Characterization by XRD showed that catalyst of H-aluminosilicate have structure amorphous, while FTIR showed Si-O-Al bond at 457 cm-1. The acidity test showed that catalyst of H-aluminosilicate have Brønsted acid site 0.0272 mmol/g and Lewis acid site 0.0005 mmol/g. Oleic acid was cracking at 340 oC for 3 and 5 hours. The product has been analyzed by GC-MS not showed compound forming biogasoline.Keywords: H-aluminosilicate, biogasoline, oleic acid ABSTRAK          Aluminosilikat dapat digunakan sebagai katalis dalam reaksi prengkahan. Pada penelitian ini telah dilakukan sintesis katalis H-aluminosilikat melalui metode hidrotermal dengan rasio Si/Al sebesar 20. Karakterisasi yang telah dilakukan meliputi uji XRD, FTIR, dan keasaman.Hasil XRD menunjukkan katalis H-aluminosilikat berbentuk amorf, sedangkan pada FTIR menunjukkan ikatan Si-O-Al pada bilangan gelombang 457 cm-1. Uji situs asam menunjukkan katalis H-aluminosilikat memiliki jumlah asam Brønsted sebesar 0.0272 mmol/g dan jumlah sisi asam Lewis sebesar 0.0005 mmol/g. Proses perengkahan asam oleat telah dilakukan pada suhu 340oC selama 3 jam dan 5 jam. Produk cracking yang diuji dengan GC-MS tidak menunjukkan pembentukan senyawa biogasoline.Kata kunci: H-aluminosilikat, biogasoline, asam oleat


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