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通过氧化物改性形成新型强碱性氮阴离子。

Formation of a New, Strongly Basic Nitrogen Anion by Metal Oxide Modification.

机构信息

Department of Applied Chemistry, Graduate School of Engineering, Tohoku University , 6-6-07 Aoba, Aramaki, Aoba-ku, Sendai 980-8579, Japan.

JST, PRESTO , 4-1-8 Honcho Kawaguchi, Saitama 332-0012, Japan.

出版信息

J Am Chem Soc. 2017 Aug 30;139(34):11857-11867. doi: 10.1021/jacs.7b05227. Epub 2017 Aug 17.

Abstract

Development of new hybrid materials having unique and unprecedented catalytic properties is a challenge for chemists, and heterogeneous-homogeneous hybrid catalysts have attracted much attention because of the preferable and exceptional properties that are highly expected to result from combination of the components. Base catalysts are widely used in organic synthesis as key materials, and a new class of base catalysts has made a large impact from academic and industrial viewpoints. Here, a principle for creating a new strong base by hybridization of homogeneous and heterogeneous components is presented. It is based on the modification of organic compounds with metal oxides by using the acid-base property of metal oxides. Based on kinetic and DFT studies, combination of CeO and 2-cyanopyridine drastically enhanced the basicity of 2-cyanopyridine by a factor of about 10 (∼9 by pK (in CHCN)), and the pK was estimated to be ∼21, which locates it in the superbase category. 2-Cyanopyridine and CeO formed a unique adsorption complex via two interaction modes: (i) coordinative interaction between the Ce atom of CeO and the N atom of the pyridine ring in 2-cyanopyridine, and (ii) covalent interaction between the surface O atom of CeO and the C atom of the CN group in 2-cyanopyridine by addition of the lattice oxygen of CeO to the CN group of 2-cyanopyridine. These interactions established a new, strongly basic site of N over the CeO surface.

摘要

开发具有独特且前所未有的催化性能的新型杂化材料是化学家面临的挑战,而多相-均相杂化催化剂因其有望结合各组分的优异性能而备受关注。碱催化剂作为关键材料广泛应用于有机合成中,一类新的碱催化剂从学术和工业角度来看都产生了重大影响。本文提出了一种通过均相和多相组分的杂交来构建新型强碱的原理。它基于利用金属氧化物的酸碱性质对有机化合物进行金属氧化物修饰。基于动力学和 DFT 研究,CeO 和 2-氰基吡啶的组合通过约 10 倍(在 CHCN 中约为 9)增强了 2-氰基吡啶的碱性,pK 被估计为约 21,这使其属于超碱类别。2-氰基吡啶和 CeO 通过两种相互作用模式形成了独特的吸附配合物:(i)CeO 的 Ce 原子与 2-氰基吡啶的吡啶环的 N 原子之间的配位相互作用,以及(ii)CeO 的表面 O 原子与 2-氰基吡啶的 CN 基团的 C 原子之间的共价相互作用,CeO 的晶格氧加成到 2-氰基吡啶的 CN 基团中。这些相互作用在 CeO 表面上建立了一个新的、强碱性的 N 位。

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