Guanosine Hydrogen-Bonded Scaffolds: A New Way to Control the Bottom-Up Realisation of Well-Defined Nanoarchitectures

被引:128
作者
Lena, Stefano [1 ]
Masiero, Stefano [1 ]
Pieraccini, Silvia [1 ]
Spada, Gian Piero [1 ]
机构
[1] Alma Mater Studiorum Univ Bologna, Dipartimento Chim Organ A Mangini, I-40126 Bologna, Italy
关键词
chirality; functional materials; guanosine; self-assembly; supramolecular chemistry; CIRCULAR-DICHROISM SPECTROSCOPY; ENANTIOMERIC SELF-RECOGNITION; DIFFUSION NMR-SPECTROSCOPY; LIQUID-CRYSTALLINE PHASE; G-QUADRUPLEX FORMATION; PI-CONJUGATED SYSTEMS; RAY FIBER DIFFRACTION; G-QUARTET; SUPRAMOLECULAR CHEMISTRY; HYDROCARBON SOLVENTS;
D O I
10.1002/chem.200802506
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Over the last two decades, guanosine-related molecules have been of interest in different areas, ranging from structural biology to medicinal chemistry, supramolecular chemistry and nanotechnology. The guanine base is a multiple hydrogen-bonding unit, capable also of binding to cations, and fits very well with contemporary studies in supramolecular chemistry, self-assembly and non-covalent synthesis. This Concepts article, after reviewing on the diversification of self-organised assemblies from guanosine-based low-molecular-weight molecules, will mainly focus on the use of guanine moiety as a potential scaffold for designing functional materials of tailored physical properties.
引用
收藏
页码:7792 / 7806
页数:15
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