Multistep organic synthesis of modular photosystems

被引:11
作者
Sakai, Naomi [1 ]
Matile, Stefan [1 ]
机构
[1] Univ Geneva, Dept Organ Chem, CH-1211 Geneva, Switzerland
来源
BEILSTEIN JOURNAL OF ORGANIC CHEMISTRY | 2012年 / 8卷
基金
欧洲研究理事会;
关键词
asparagusic acid; charge-transfer cascades; chromophores; disulfide exchange; hydrazone exchange; molecular switches; naphthalenediimides; pi-stacks; surface-initiated polymerization; SURFACE-INITIATED POLYMERIZATION; DOUBLE-CHANNEL PHOTOSYSTEMS; ELECTRON-TRANSFER; CORE; NAPHTHALENEDIIMIDE; EXCHANGE; SEMICONDUCTORS; DISULFIDE; CHEMISTRY; DONOR;
D O I
10.3762/bjoc.8.102
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Quite extensive synthetic achievements vanish in the online supporting information of publications on functional systems. Underappreciated, their value is recognized by experts only. As an example, we here focus in on the recent synthesis of multicomponent photosystems with antiparallel charge-transfer cascades in co-axial hole- and electron-transporting channels. The synthetic steps are described one-by-one, starting with commercial starting materials and moving on to key intermediates, such as asparagusic acid, an intriguing natural product, as well as diphosphonate "feet", and panchromatic naphthalenediimides (NDIs), to finally reach the target molecules. These products are initiators and propagators for self-organizing surface-initiated polymerization (SOSIP), a new method introduced to secure facile access to complex architectures. Chemoorthogonal to the ring-opening disulfide exchange used for SOSIP, hydrazone exchange is then introduced to achieve stack exchange, which is a "switching" technology invented to drill giant holes into SOSIP architectures and fill them with functional pi-stacks of free choice.
引用
收藏
页码:897 / 904
页数:8
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