Novel photoactive transition metal catalysts for the UV-Light-Triggered Metathesis Polymerization of Functional Monomers

用于紫外光触发功能单体复分解聚合的新型光活性过渡金属催化剂

基本信息

项目摘要

This project aims on the synthesis of novel ruthenium-based metal complexes that shall serve as photo-active precursors for metathesis catalysts. These organometallic compounds shall be based on Ru-N-heterocyclic carbenes with additional ligands that can be selectively removed upon irradiation with UV-light (¿ < 300 nm). Important enough and in contrast to (few) existing systems, these precursor compounds shall be stable at temperatures up to 45°C and to irradiation with visible light (¿ > 300 nm). Complexes activated by light with ¿ < 300 nm shall be exposed to strained olefins such as functional norborn-2-enes and cyclooctenes to form ring-opening metathesis polymerization (ROMP) active catalysts. Complementary, the activated complexes shall be reacted with various functional 1,6-heptadiynes to form cyclopolymerization active species to gain access to semiconducting and conducting species. Investigations on the mechanism of activation as well as kinetic measurements shall be carried out. Finally, the novel systems shall be used to create x/y-resolved surface-immobilized polymer brushes as well as x/y-resolved surface-bound (semi-) conducting polymers layers and wires. These shall be used for the realization of bioanalytic devices, e.g. for DNA analysis. Conductive layers shall be used for the construction of (semi-) conducting polymer layers.
本项目的目标是合成新型的铼基金属配合物,作为复分解催化剂的光活性前体。这些有机金属化合物应基于具有额外配体的Ru-N-杂环卡宾,所述额外配体可在用UV光(λ < 300 nm)照射时选择性地去除。足够重要的是,与(少数)现有系统相比,这些前体化合物在高达45°C的温度下和可见光(> 300 nm)的照射下应保持稳定。通过λ < 300 nm的光活化的复合物应暴露于应变烯烃如官能降冰片-2-烯和环辛烯以形成开环易位聚合(ROMP)活性催化剂。互补地,活化的络合物应与各种官能的1,6-庚二炔反应以形成环聚合活性物质,从而获得半导体和导电物质。应进行活化机制的研究以及动力学测量。最后,新的系统将用于创建x/y-分辨的表面固定的聚合物刷以及x/y-分辨的表面结合的(半)导电聚合物层和电线。这些应用于实现生物分析设备,例如用于DNA分析。导电层应用于(半)导电聚合物层的构造。

项目成果

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Professor Dr. Michael R. Buchmeiser其他文献

Professor Dr. Michael R. Buchmeiser的其他文献

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{{ truncateString('Professor Dr. Michael R. Buchmeiser', 18)}}的其他基金

High Oxidation State Tungsten Oxo, Tungsten Thio, and Tungsten Imido Alkylidene NHC Complexes for Olefin Metathesis of Functional Olefins
高氧化态氧化钨、硫代钨和亚氨基亚烷基钨 NHC 配合物用于功能性烯烃的烯烃复分解
  • 批准号:
    319116190
  • 财政年份:
    2016
  • 资助金额:
    --
  • 项目类别:
    Research Grants
Functional Group Tolerant Olefin Metathesis Catalysts Based on N-Heterocyclic Carbene Complexes of High Oxidation State Molybdenum Imido Alkylidenes
基于高氧化态亚氨基钼亚烷基N-杂环卡宾配合物的官能团耐受性烯烃复分解催化剂
  • 批准号:
    271749009
  • 财政年份:
    2015
  • 资助金额:
    --
  • 项目类别:
    Research Grants
High Modulus and High Strength C/C-SiC Ceramic Matrix Composites by Fiber-Matrix Interface Tailoring via Modification of Fiber Surface and Matrix Precursor - Kerafam 2
通过纤维表面和基体前驱体改性实现纤维基体界面定制的高模量和高强度 C/C-SiC 陶瓷基复合材料 - Kerafam 2
  • 批准号:
    277680365
  • 财政年份:
    2015
  • 资助金额:
    --
  • 项目类别:
    Research Grants
Polymerization Catalysts for the Reversible Switching Between Vinyl Insertion and Ring-Opening Metathesis Polymerization
用于乙烯基插入和开环复分解聚合之间可逆转换的聚合催化剂
  • 批准号:
    226688656
  • 财政年份:
    2012
  • 资助金额:
    --
  • 项目类别:
    Research Grants
Metathesis under Biphasic Conditions Using Monolithic-Supported Ionic Liquids
使用整体支撑离子液体在双相条件下进行复分解
  • 批准号:
    136355964
  • 财政年份:
    2010
  • 资助金额:
    --
  • 项目类别:
    Research Grants
Regio- and Stereoselective Cyclopolymerization of Functional 1,6-Heptadiynes and 1,5-Hexadiynes: Rationalizing Catalyst Activity with Monomer Structure
功能性 1,6-庚二炔和 1,5-己二炔的区域和立体选择性环聚合:通过单体结构合理化催化剂活性
  • 批准号:
    41694162
  • 财政年份:
    2007
  • 资助金额:
    --
  • 项目类别:
    Research Grants
Monolithisch-geträgerte Metall-Nanocluster für katalytische Anwendungen
用于催化应用的整体支撑金属纳米团簇
  • 批准号:
    20805014
  • 财政年份:
    2006
  • 资助金额:
    --
  • 项目类别:
    Research Grants
Origin of Differences in Regioselectivity in the (Cyclo-) Polymerization of alpha, omega-Diynes and 1-Alkynes Between Tetra- and Penta-Coordinated Mo/W Imido/Oxo Alkylidene N-Heterocyclic Carbene Complexes and Implications for Ene-yne Metathesis
四配位和五配位Mo/W亚氨基/氧代亚烷基N-杂环卡宾配合物之间α、omega-二炔和1-炔烃的(环)聚合中区域选择性差异的起源及其对烯-炔复分解的影响
  • 批准号:
    449377332
  • 财政年份:
  • 资助金额:
    --
  • 项目类别:
    Research Grants

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CAS:能够还原和氧化降解全氟烷基物质的光活性共价有机框架的分子设计
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为高效碳基钙钛矿光伏电池创建新型电极-光活性层混合结构
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博士后奖学金:MPS-Ascend:用于多氟烷基和全氟烷基物质的封存和降解的光活性金属有机纳米笼
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