EXPLORATION OF COPPER-BASED COORDINATION POLYMER AS CATALYST: HIGH YIELD OXIDATIVE COUPLING OF BENZYLAMINE TO IMINE

IF 0.5 Q4 EDUCATION & EDUCATIONAL RESEARCH
Aieshri Swargiary
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引用次数: 0

Abstract

Benzylamine to imine conversion through oxidative coupling reaction has been achieved with almost 91% yield under very mild conditions by applying a one-dimensional coordination polymer as a catalyst and tert-butyl hydroperoxide (TBHP) as an oxidizing agent. The 1D-coordination polymer, [{Cu2(2,3-pydc)2(2,2ʹ-bpy) (H2O)2}.4H2O]n(A) has been re-synthesized by different synthetic process using the ligands 2,3- pyridinedicarboxylic acid (2,3-pydc) and 2,2Ꞌ-bipyridine (2,2Ꞌ-bpy) and it has been characterized by utilizing different physicochemical techniques such as IR-spectroscopy, UV-Vis spectroscopy, elemental analysis and TGDTA analysis including reestablishment of X-ray single crystal structure. The proposed mechanism of the reaction indicates that the catalytic reaction is facilitated by a flexible and coordinatively unsaturated Cu(II) center and through the formation of tert-butyl peroxy radical.
铜基配位聚合物催化苯胺与亚胺高收率氧化偶联的探索
以一维配位聚合物为催化剂,过氧化叔丁基(TBHP)为氧化剂,在非常温和的条件下,通过氧化偶联反应将苯胺转化为亚胺,收率接近91%。以2,3-吡啶二羧酸(2,3-pydc)和2,2Ꞌ-联吡啶(2,2Ꞌ-bpy)为配体,通过不同的合成工艺重新合成了一维配位聚合物[{Cu2(2,3-pydc)2(2,2 -pydc) (H2O)2}. 4h2o]n(A),并利用不同的物理化学技术,如红外光谱、紫外-可见光光谱、元素分析和TGDTA分析(包括重建x射线单晶结构)对其进行了表征。提出的反应机理表明,灵活的配位不饱和Cu(II)中心和叔丁基过氧自由基的形成促进了催化反应。
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来源期刊
Rasayan Journal of Chemistry
Rasayan Journal of Chemistry Energy-Energy (all)
CiteScore
1.90
自引率
0.00%
发文量
196
期刊介绍: RASĀYAN Journal of Chemistry [RJC] signifies a confluence of diverse streams of chemistry to stir up the cerebral powers of its contributors and readers. By introducing the journal by this name, we humbly intent to provide an open platform to all researchers, academicians and readers to showcase their ideas and research findings among the people of their own fraternity and to share their vast repository of knowledge and information. The journal seeks to embody the spirit of enquiry and innovation to augment the richness of existing chemistry literature and theories. We also aim towards making this journal an unparalleled reservoir of information and in process aspire to inculcate and expand the research aptitude.
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