检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
作 者:张荷兰[1] 晏妮[1] 武思文[1] 蔡秀琴[1] 刘凯强[1] 房喻[1]
机构地区:[1]应用表面与胶体化学教育部重点实验室,陕西师范大学化学与材料科学学院,西安710062
出 处:《高等学校化学学报》2011年第7期1573-1580,共8页Chemical Journal of Chinese Universities
基 金:国家自然科学基金(批准号:20902055,91027017)资助
摘 要:以甘氨酸为连接臂、顺反丁烯二酸为功能基团设计合成了2种具有不同立体异构连接臂的A(LS)2型双胆固醇类小分子胶凝剂MA-C和FA-C.考察了MA-C和FA-C对30种常见有机溶剂的胶凝能力.结果表明,MA-C和FA-C的胶凝能力及其所形成凝胶的性质依赖于胶凝剂分子的立体异构.特别是MA-C能使CCl4室温胶凝,而且所形成凝胶具有良好的热稳定性和显著的剪切触变性.另外,此胶凝剂还能在H2O/CCl4混合体系中选择胶凝有机相.显微分析表明,凝胶中胶凝剂聚集体的形貌不仅依赖于胶凝剂分子的立体异构和胶凝剂的浓度,而且与胶凝剂分子与溶剂分子间的相互作用有关.变温、变浓度的1H NMR研究表明,胶凝剂分子间的π-π堆积和氢键作用是凝胶形成的重要驱动力.此外,根据XRD和其它实验结果提出了MA-C在CCl4中的可能堆积模型.Two cholesterol-containing low molecular mass gelators(LMMGs) of A(LS)2 type with glycin in the linkers and butene diacid in the A part were prepared.Their gelation abilities were evaluated in 30 commonly used organic solvents.It was found that the change in the stereo-structure of the linker had a dramatic effect upon the gelation behaviors of the gelators.Interestingly,MA-C gelated CCl4 spontaneously at room temperature,and the gel as-formed exhibited good thermal stability and thixotropic property as revealed by rheological studies.More interestingly,MA-C showed phase-selective gelation of CCl4 from its mixture with water.SEM observation demonstrated that the morphologies of the aggregates of the gelators in the gels depend,but not only,on the structures of the gelators.The concentrations of the gelators,and even their interactions with the solvents also showed great effect upon the morphologies.Temperature and concentration dependent 1H NMR measurements revealed that inter-molecular hydrogen bonding and π-π stacking among the molecules of the gelators are important driving forces for the formation of the gels.XRD study revealed that MA-C assembled into a layered structure in its CCl4 gel.
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:18.119.100.196