| Preface | 第1-9页 |
| Chapter I Introduction | 第9-51页 |
| ·Introduction | 第9-10页 |
| ·Classification of organogelators | 第10-20页 |
| ·The fatty acid derivatives and simple organogelators | 第10-11页 |
| ·Steroid and cholesterol-based organogelators | 第11-13页 |
| ·Anthryl derivatives and ALS gelators | 第13-14页 |
| ·OPVs derivatives | 第14-15页 |
| ·Other kinds of organogelators | 第15-17页 |
| ·Two-component organogelators | 第17-20页 |
| ·The measurement for organogel phase’s characterization | 第20-32页 |
| ·The driving forces behind the organogelation | 第21-26页 |
| ·Evidence of H-bonding: FT-IR, ~1H NMR | 第21-23页 |
| ·Evidences of π-stacking, dipolar and van der Waals interactions: 1H NMR and electronic spectral tests | 第23-26页 |
| ·Morphologies and structures investigation: SEM, TEM, AFM, OPM, CLS and S/WXRD | 第26-28页 |
| ·CD, DSC, and rheological measurements | 第28-31页 |
| ·Modulation of the photophysical properties of organogels | 第31-32页 |
| ·Potential applications of organogels | 第32-41页 |
| ·Gels as structure directing agents for the synthesis of inorganic nanostructures | 第33-34页 |
| ·Energy transfer and light harvesting in organogels | 第34-37页 |
| ·Smart gel: sensitive to external stimuli | 第37-39页 |
| ·Other functions of organogels | 第39-41页 |
| Liquid crystalline physical gels | 第39页 |
| Gel electrolytes | 第39-40页 |
| Gel for noncopyable fluorescent imaging | 第40-41页 |
| ·The background and the design | 第41-42页 |
| ·References | 第42-51页 |
| Chapter II A Potent Triphenylbenzene-based H-bonding Donor to Assist Formation of Two-component Organogels with Stilbazoles | 第51-72页 |
| ·Introduction | 第51-52页 |
| ·Synthesis and structures of complexes | 第52-54页 |
| ·Results and discussion | 第54-64页 |
| ·Gelation behaviour of 3 and complexes A, B, C and D | 第54-55页 |
| ·Sol-gel phase transition temperatures | 第55-56页 |
| ·Scanning Electron Microscopy (SEM) and small angle X-ray Diffraction (XRD) Patterns | 第56-59页 |
| ·UV-vis absorption and FT-IR spectroscopy analyses | 第59-61页 |
| ·Variable temperature 1H NMR spectroscopy study of Complex C DMSO gel | 第61-62页 |
| ·Fluorescence emission spectra | 第62-64页 |
| ·Conclusion | 第64-65页 |
| ·References | 第65-70页 |
| ~1H and ~13C NMR spectra | 第70-72页 |
| Chapter III Strategy to control the chromism and fluorescence emission of a perylene dye in composite organogel phases | 第72-96页 |
| ·Introduction | 第72-73页 |
| ·Synthesis | 第73-74页 |
| ·Results and discussion | 第74-87页 |
| ·The self-assembling properties: SEM, XRD and FMI measurements | 第74-77页 |
| ·The chromism properties of the gel phases: Uv-vis absorption, fluorescence excitation, rheological and Tgel measurements | 第77-82页 |
| ·Controllable fluorescence emission | 第82-85页 |
| ·Resonance Emission Transfer (RET) | 第85-87页 |
| Calculation of efficiency and the rate constant of energy transfer | 第86-87页 |
| ·Conclusion | 第87-88页 |
| ·References | 第88-94页 |
| Supplementary figures and 1H NMR spectrum | 第94-96页 |
| Chapter IV Self-assembly of C3-Symmetrical Cyano-Substituted Triphenylbenzenes in Different Solvents: Fabrication of Organogels and Organic Nanospheres with Controllable Fluorescence Emission | 第96-126页 |
| ·Introduction | 第96-97页 |
| ·Synthesis | 第97-100页 |
| ·Results and discussion | 第100-112页 |
| ·Gelation ability | 第100-101页 |
| ·SEM morphological observation | 第101-103页 |
| ·Small angle X-ray diffraction measurements | 第103-104页 |
| ·FT-IR spectra | 第104-106页 |
| ·UV vis absorption and fluorescence excitation spectra | 第106-108页 |
| ·Fluorescence emissions of gel and sol phases | 第108-110页 |
| ·Emission changes in organic nanospheres based on CN-DBAPPB3 and CN-DBAPP82 | 第110-112页 |
| ·Conclusion | 第112-113页 |
| ·References | 第113-120页 |
| Supplementary figures and 1H NMR spectra | 第120-126页 |
| Experimental instruments | 第126-128页 |
| Publications | 第128-129页 |
| Acknowledgements | 第129-130页 |
| Abstract | 第130-133页 |
| 中文摘要 | 第133-134页 |
