摘 要：分子自組裝是分子自發(fā)形成特定有序聚集結(jié)構(gòu)的過(guò)程。為了建立新的功能自組裝體系，實(shí)現(xiàn)分子聚集體由單組分到多組分、由靜態(tài)到動(dòng)態(tài)，并通過(guò)環(huán)境變化進(jìn)而實(shí)現(xiàn)從聚集體結(jié)構(gòu)可控發(fā)展到功能可控，在過(guò)去一年里，我們從無(wú)機(jī)金屬氧簇和與之匹配的有機(jī)組分構(gòu)筑基元設(shè)計(jì)入手，通過(guò)組分間結(jié)構(gòu)匹配和作用方式、組裝性質(zhì)、刺激響應(yīng)及功能特性調(diào)節(jié)，合成了一系列新的以無(wú)機(jī)簇陰離子為核、以修飾的有機(jī)陽(yáng)離子為殼的雙組分通過(guò)靜電相互作用形成的、具有刺激響應(yīng)性和適應(yīng)不同功能需要的、結(jié)構(gòu)形態(tài)可變的兩親性超分子復(fù)合物預(yù)組裝體。我們以研究復(fù)合物自組裝形成的多級(jí)聚集結(jié)構(gòu)為基礎(chǔ)，通過(guò)揭示響應(yīng)基團(tuán)與組裝結(jié)構(gòu)間的聯(lián)動(dòng)關(guān)系，獲得了具有可逆轉(zhuǎn)變特性的分子組裝體并闡明了動(dòng)態(tài)轉(zhuǎn)變過(guò)程和機(jī)理。在此基礎(chǔ)上，我們利用溶液中組裝結(jié)構(gòu)的動(dòng)態(tài)可調(diào)控特性，通過(guò)光照和溫度變化調(diào)控分子間相互作用，實(shí)現(xiàn)了水相中分子聚集體的組裝與解組裝、極性相和非極性相之間的可逆相轉(zhuǎn)移、可逆氧化還原和相轉(zhuǎn)移催化氧化功能。該年度的工作實(shí)現(xiàn)了將有機(jī)和無(wú)機(jī)組分通過(guò)多種相互作用整合到同一個(gè)組裝體系中，揭示了多金屬氧簇超分子復(fù)合物的手性轉(zhuǎn)移和可逆光致變色、手性組裝結(jié)構(gòu)與非手性組裝結(jié)構(gòu)的動(dòng)態(tài)結(jié)構(gòu)可逆轉(zhuǎn)變和機(jī)理，同時(shí)實(shí)現(xiàn)了同時(shí)含有主體和客體基團(tuán)的超分子復(fù)合物自識(shí)別、手性轉(zhuǎn)移和手性放大的光調(diào)控。這些工作將為實(shí)現(xiàn)該研究的下一步目標(biāo)提供很好的基礎(chǔ)。

關(guān)鍵詞：有機(jī)-無(wú)機(jī)復(fù)合體系 自組裝 分子聚集體 動(dòng)態(tài)調(diào)控 功能

Abstract： Molecular self-assembly is the process that molecules or molecular groups spontaneous form specific aggregation structure. New functional self-assembly systems with the molecular aggregations changing from monocomponent to multicomponent， from static structure to dynamic evolution， and from structural control to functional adjustment， through the stimulus of outside environment， have now become challenges and the coming goals. To match the purpose of the present project， we start to design new type of building block bearing inorganic polyoxometalate clusters and organic functional units. Through the regulation of matched structures and interactions among these components， the dynamic assembly and stimuli-response properties are investigated by variable shape and amphiphilicity of the supramolecular complexes which contain inorganic clusters as the core and surface modified organic cations as the shell. From the obtained multilevel aggregation structures constructed by the self-assembly of the complexes， we demonstrate the relationship between responsive groups and assembly structures. Following these understanding， we achieve dynamic assemblies with reversible transformation characteristics， and further identify their transformation process and mechanism. On the basis of this， we have taken advantage of dynamic controllable characteristics of assembled structures， through adjusting the molecule interaction by temperature and light in solution， and finally realize phase transfer， redox and catalytic oxidation of assemblies under mild conditions. The job of this year integrates various components in one assembly system through multiple interactions. We uncovered chiral transfer and reversible photochromism， reversible transformation of helical and spherical assembled structures and the possible mechanism. Meanwhile， we have realized the photo-modulation for the self-recognization， chiral transfer and amplification of dynamic reversible self-assemblies of an inorganic/organic complex bearing host and guest simultaneously. All the present research results pave the strong base for the realization of the next targets.

Key Words： Organic-Inorganic Complex system； Self-Assembly； Molecular aggregation； Dynamic control； Function

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