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室温下由 Ru(cod)(cot)前体原位形成的催化活性钌纳米催化剂催化氨硼烷脱氢/脱氢偶联反应。

In situ formed catalytically active ruthenium nanocatalyst in room temperature dehydrogenation/dehydrocoupling of ammonia-borane from Ru(cod)(cot) precatalyst.

机构信息

Department of Chemistry, Yüzüncü Yıl University, Van, Turkey.

出版信息

Langmuir. 2012 Mar 20;28(11):4908-14. doi: 10.1021/la2049162. Epub 2012 Mar 5.

Abstract

The development of simply prepared and effective catalytic materials for dehydrocoupling/dehydrogenation of ammonia-borane (AB; NH(3)BH(3)) under mild conditions remains a challenge in the field of hydrogen economy and material science. Reported herein is the discovery of in situ generated ruthenium nanocatalyst as a new catalytic system for this important reaction. They are formed in situ during the dehydrogenation of AB in THF at 25 °C in the absence of any stabilizing agent starting with homogeneous Ru(cod)(cot) precatalyst (cod = 1,5-η(2)-cyclooctadiene; cot = 1,3,5-η(3)-cyclooctatriene). The preliminary characterization of the reaction solutions and the products was done by using ICP-OES, ATR-IR, TEM, XPS, ZC-TEM, GC, EA, and (11)B, (15)N, and (1)H NMR, which reveal that ruthenium nanocatalyst is generated in situ during the dehydrogenation of AB from homogeneous Ru(cod)(cot) precatalyst and B-N polymers formed at the initial stage of the catalytic reaction take part in the stabilization of this ruthenium nanocatalyst. Moreover, following the recently updated approach (Bayram, E.; et al. J. Am. Chem. Soc.2011, 133, 18889) by performing Hg(0), CS(2) poisoning experiments, nanofiltration, time-dependent TEM analyses, and kinetic investigation of active catalyst formation to distinguish single metal or in the present case subnanometer Ru(n) cluster-based catalysis from polymetallic Ru(0)(n) nanoparticle catalysis reveals that in situ formed Ru(n) clusters (not Ru(0)(n) nanoparticles) are kinetically dominant catalytically active species in our catalytic system. The resulting ruthenium catalyst provides 120 total turnovers over 5 h with an initial turnover frequency (TOF) value of 35 h(-1) at room temperature with the generation of more than 1.0 equiv H(2) at the complete conversion of AB to polyaminoborane (PAB; NH(2)BH(2)) and polyborazylene (PB; NHBH) units.

摘要

在温和条件下,开发简单制备和高效的氨硼烷(AB;NH(3)BH(3))脱氢/脱氢催化材料仍然是氢能经济和材料科学领域的一个挑战。本文报道了原位生成的钌纳米催化剂作为这一重要反应的新型催化体系的发现。它们是在 25°C 的四氢呋喃中 AB 脱氢时原位形成的,起始于均相 Ru(cod)(cot)前催化剂,没有任何稳定剂(cod = 1,5-η(2)-环辛二烯;cot = 1,3,5-η(3)-环辛三烯)。通过使用 ICP-OES、ATR-IR、TEM、XPS、ZC-TEM、GC、EA 和 (11)B、(15)N 和 (1)H NMR 对反应溶液和产物进行初步表征,发现 Ru 纳米催化剂是由均相 Ru(cod)(cot)前催化剂和催化反应初始阶段形成的 B-N 聚合物在 AB 脱氢过程中原位生成的,并且形成的 B-N 聚合物参与了 Ru 纳米催化剂的稳定。此外,根据最近更新的方法(Bayram,E.;等人。J. Am. Chem. Soc.2011, 133, 18889),通过进行 Hg(0)、CS(2) 中毒实验、纳滤、时变 TEM 分析和活性催化剂形成的动力学研究,以区分单金属或在本例中基于亚纳米 Ru(n)簇的催化与多金属 Ru(0)(n)纳米颗粒催化,表明原位形成的 Ru(n)簇(不是 Ru(0)(n)纳米颗粒)是我们催化体系中动力学上占主导地位的催化活性物种。在室温下,得到的钌催化剂在 5 小时内提供了 120 次总转化,初始转化频率(TOF)值为 35 h(-1),在 AB 完全转化为多氨基硼烷(PAB;NH(2)BH(2))和聚硼氮烷(PB;NHBH)单元时,生成超过 1.0 当量的 H(2)。

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