永利“当代科学前沿讲坛”第228讲 The Breaking and Mending of Porphyrins: Synthesis of Porphyrinoids Incorporating Non-Pyrrolic Heterocycles

创建时间:  2016/06/24  龚惠英   浏览次数:   返回

永利"当代科学前沿讲坛"第228讲  [摘要]

报告题目:The Breaking and Mending of Porphyrins: Synthesis of Porphyrinoids Incorporating Non-Pyrrolic Heterocycles
报 告 人:Christian Brückner教授(美国康涅狄格大学)
报告时间:2016年6月30号(周四)10:00
报告地点:校本部HA102
邀 请 人:张展教授
主办单位:永利化学系
报告简介:Naturally occurring porphyrins and hydroporphyrins vary with respect to their ring substituents and oxidation states, but their tetrapyrrolic frameworks remain fully preserved across all kingdoms of life; there are no naturally occurring porphyrin-like macrocycles known that contain non-pyrrolic building blocks. The modulation of the electronic properties of porphyrins–particularly with respect to their wavelengths of absorption and emission–is desirable for their utilization in numerous technical and medical applications. Our group developed synthetic strategies toward the conversion of one or two pyrrolic building blocks in porphyrins into different 4-, 5-, and 6-membered heterocycles, forming so-called 'pyrrole-modified porphyrins'. We report on the scope and limits of applying class ring expansion reactions to expanding a pyrrole within the steric constraints of the porphyrinic macrocycle. We will describe to which extend these modifications affect the chemical reactivity, conformation, conformational flexibility, and photochemical properties of the resulting porphyrin-, chlorin-, and bacteriochlorin-analogues. The utilization of the chromophores in chemosensing and optical and photo-acoustic imaging applications is briefly highlighted.

上一条:数学系Seminar第1325期 关于带科里奥利效应的浅水波模型的渐近分析

下一条:数学系Seminar第1326期 一些来自于水波的拟线性方程的爆破解


永利“当代科学前沿讲坛”第228讲 The Breaking and Mending of Porphyrins: Synthesis of Porphyrinoids Incorporating Non-Pyrrolic Heterocycles

创建时间:  2016/06/24  龚惠英   浏览次数:   返回

永利"当代科学前沿讲坛"第228讲  [摘要]

报告题目:The Breaking and Mending of Porphyrins: Synthesis of Porphyrinoids Incorporating Non-Pyrrolic Heterocycles
报 告 人:Christian Brückner教授(美国康涅狄格大学)
报告时间:2016年6月30号(周四)10:00
报告地点:校本部HA102
邀 请 人:张展教授
主办单位:永利化学系
报告简介:Naturally occurring porphyrins and hydroporphyrins vary with respect to their ring substituents and oxidation states, but their tetrapyrrolic frameworks remain fully preserved across all kingdoms of life; there are no naturally occurring porphyrin-like macrocycles known that contain non-pyrrolic building blocks. The modulation of the electronic properties of porphyrins–particularly with respect to their wavelengths of absorption and emission–is desirable for their utilization in numerous technical and medical applications. Our group developed synthetic strategies toward the conversion of one or two pyrrolic building blocks in porphyrins into different 4-, 5-, and 6-membered heterocycles, forming so-called 'pyrrole-modified porphyrins'. We report on the scope and limits of applying class ring expansion reactions to expanding a pyrrole within the steric constraints of the porphyrinic macrocycle. We will describe to which extend these modifications affect the chemical reactivity, conformation, conformational flexibility, and photochemical properties of the resulting porphyrin-, chlorin-, and bacteriochlorin-analogues. The utilization of the chromophores in chemosensing and optical and photo-acoustic imaging applications is briefly highlighted.

上一条:数学系Seminar第1325期 关于带科里奥利效应的浅水波模型的渐近分析

下一条:数学系Seminar第1326期 一些来自于水波的拟线性方程的爆破解

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