...
首页> 外文期刊>Polyhedron: The International Journal for Inorganic and Organometallic Chemistry >Liquid phase versus microwave assisted selective oxidation of volatile organic compounds involving dioxidomolybdenum(VI) and oxidoperoxidomolybdenum(VI) complexes as catalysts in the presence/absence of an N-based additive
【24h】

Liquid phase versus microwave assisted selective oxidation of volatile organic compounds involving dioxidomolybdenum(VI) and oxidoperoxidomolybdenum(VI) complexes as catalysts in the presence/absence of an N-based additive

机译:在存在/不存在基于N的添加剂的情况下,液相与微波辅助选择性氧化涉及二氧化钼(VI)和氧化过氧化钼(VI)配合物的挥发性有机化合物

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

Four dioxidomolybdenum(VI) complexes, [(MoO2)-O-VI(dha-bhz)(MeOH)]center dot(H(2)dha-bhz) (1), [MoO2(dha-inh) (MeOH)] (2), [MoO2(dha-nah)(MeOH)] (3) and [MoO2(dha-fah)(MeOH)] (4), and their corresponding oxidoperoxidomolybdenum(VI) complexes, [MoO(O-2)(dha-bhz)(MeOH)] (5), [MoO(O-2)(dha-inh)(MeOH)] (6), [MoO(O-2)(dha-nah)(MeOH)] (7) and [Mo(O-2)(dha-fah)(MeOH)] (8), with ONO tridentate Schiff base ligands derived from 3-acetyl-6-methyl-(2H)-pyran-2,4(3H)-dione (dehydroacetic acid, Hdha) and aromatic hydrazides, {benzoyl hydrazide (bhz), isonicotinoyl hydrazide (inh), nicotinoyl hydrazide (nah) and furoyl hydrazide (fah)} have been synthesized and characterized by elemental analysis, spectroscopic techniques (infrared, UV-Vis, H-1 and C-13 NMR) and thermogravimetric analyses. The structures of complexes 1 and 2, confirmed by single crystal X-ray study, reveal that the tridentate ligand binds to the metal centers through the enolic oxygen (of the pyrone group), azomethine nitrogen and enolic oxygen (of the hydrazide group) atoms; methanol is coordinated at one site through the oxygen atom. The dioxidomolybdenum(VI) complexes have been tested as catalysts for the homogeneous oxidation of secondary alcohols (1-phenyl ethanol, 2-propanol and 2-butanol), using 30% H2O2 as an oxidant. Both microwave and conventional liquid phase oxidation methods have been tested for catalytic reactions. Various parameters, such as amount of catalyst, oxidant, solvent and temperature, of the reaction mixture have been taken into consideration for the maximum conversion of the substrates. Under the atmospheric optimized reaction conditions, secondary alcohols give high yields of the respective ketones selectively. Addition of an N-based additive reduces the time and increases the conversion of alcohols. Amongst the two methods studied, the microwave technique proves to be a time efficient system. (C) 2015 Elsevier Ltd. All rights reserved.
机译:四种双氧钼(VI)配合物,[(MoO2)-O-VI(dha-bhz)(MeOH)]中心点(H(2)dha-bhz)(1),[MoO2(dha-inh)(MeOH)] (2),[MoO2(dha-nah)(MeOH)](3)和[MoO2(dha-fah)(MeOH)](4),及其相应的氧化过氧化钼(VI)络合物,[MoO(O-2) (dha-bhz)(MeOH)](5),[MoO(O-2)(dha-inh)(MeOH)](6),[MoO(O-2)(dha-nah)(MeOH)]( 7)和[Mo(O-2)(dha-fah)(MeOH)](8),以及源自3-乙酰基-6-甲基-(2H)-吡喃-2,4(3H)的ONO三齿席夫碱配体)-二酮(脱氢乙酸,Hdha)和芳族酰肼,{苯甲酰酰肼(bhz),异烟酰酰肼(inh),烟酰酰肼(nah)和呋喃酰酰肼(fah)}已合成并通过元素分析,光谱技术(红外,UV-Vis,H-1和C-13 NMR)和热重分析。配合物1和2的结构通过单晶X射线研究证实,表明三齿配体通过(吡喃基)烯醇氧,(甲酰肼基)偶氮甲氮和烯醇氧原子与金属中心结合;甲醇在一个位置通过氧原子配位。使用30%的H2O2作为氧化剂,已经测试了二氧化钼(VI)络合物作为仲醇(1-苯基乙醇,2-丙醇和2-丁醇)均相氧化的催化剂。微波和常规液相氧化方法都已经过催化反应的测试。为了使底物的最大转化率,已经考虑了反应混合物的各种参数,例如催化剂的量,氧化剂,溶剂和温度。在大气优化的反应条件下,仲醇选择性地产生高产率的相应酮。添加基于N的添加剂可减少时间并增加醇的转化率。在所研究的两种方法中,微波技术被证明是一种省时的系统。 (C)2015 Elsevier Ltd.保留所有权利。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号