Skeletal Ni catalysts were prepared from Ni-Zr alloys, which possess different chemical composition and atomic arrangements, by a combination of thermal treatment and treatment with aqueous HF. Hydrogen generation from ammonia borane over the skeletal Ni catalysts proceeded efficiently, whereas the amorphous Ni-Zr alloy was inactive. Skeletal Ni prepared from amorphous Ni30 Zr70 alloy had a higher catalytic activity than that prepared from amorphous Ni40 Zr60 and Ni50 Zr50 alloys. The atomic arrangement of the Ni-Zr alloy also strongly affected the surface structure and catalytic activities. Thermal treatment of the amorphous Ni-Zr alloys at a temperature slightly lower than the crystallization temperature led to an increase of the number of surface-exposed Ni atoms and an enhancement of the catalytic activities for hydrogen generation from ammonia borane. The skeletal Ni catalysts also showed excellent durability and recyclability.

Download full-text PDF

Source
http://dx.doi.org/10.1002/cphc.201500964DOI Listing

Publication Analysis

Top Keywords

skeletal catalysts
16
prepared amorphous
12
amorphous ni-zr
12
ni-zr alloys
12
hydrogen generation
12
generation ammonia
12
ammonia borane
12
borane skeletal
12
catalysts prepared
8
thermal treatment
8

Similar Publications

Z-scheme CeO-TiO@CNT (CTC) heterojunction is fabricated using hydrothermal method and evaluated for removing mixed pollutants (MIX-P) from ciprofloxacin (CPF) and textile contaminations. CTC demonstrated ≈99% removal efficiency against MIX-P under solar irradiation of ≈10 lumens. High removal efficiency of CTC is attributed to reduced bandgap (E), 2.

View Article and Find Full Text PDF

Development of Continuous-Flow Reactions for the Synthesis of Anti-Alzheimer Drug Memantine.

Chemistry

November 2024

Department of Chemistry, School of Science, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-0033, Japan.

Memantine hydrochloride, a non-competitive antagonist of NMDA-type glutamate receptors, is known to suppress the progression of symptoms in Alzheimer's disease. Possessing a characteristic adamantane skeleton as its core structure and an amino group at the bridgehead position, memantine was synthesized starting from acenaphthene. The synthesis involved nucleus hydrogenation of acenaphthene to perhydroacenaphthene, skeletal rearrangement of perhydroacenaphthene, nitration of 1,3-dimethyladamantane, and reduction of the nitro groups to an amino group.

View Article and Find Full Text PDF
Article Synopsis
  • The first Clinical and Scientific Conference on ADSS1 myopathy took place on June 3, 2024, at NIH in Maryland, focusing on this rare inherited neuromuscular disease.
  • The conference highlighted geographical patient clusters from South Korea, Japan, India, and the USA, along with research on pre-clinical models to better understand the disease.
  • Experts identified biochemical pathways for potential therapies and created an ADSS1 myopathy consortium to guide new treatment development.
View Article and Find Full Text PDF

Biodegradable metals based on zinc are being developed to serve as temporary arterial scaffolding. Although the inclusion of copper is becoming more prevalent for grain refinement in zinc alloys, the biological activity of the copper component has not been well investigated. Here, two ZnCu alloys (0.

View Article and Find Full Text PDF

Split cross-coupling via Rh-catalysed activation of unstrained aryl-aryl bonds.

Nat Catal

April 2024

Department of Chemistry, University of Chicago, Chicago, Illinois 60637, United States.

Constructive functionalization of unstrained aryl-aryl bonds has been a fundamental challenge in organic synthesis due to the inertness of these bonds. Here we report a split cross-coupling strategy that allows two-fold arylation with diverse aryl iodides through cleaving unstrained aryl-aryl bonds of common 2,2'-biphenols. The reaction is catalyzed by a rhodium complex and promoted by a removable phosphinite directing group and an organic reductant.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!