Their gelation behaviors in 23 kinds of organic solvents have been investigated. The formed organogels can be regulated by changing the flexible/rigid segments in spacers and organic solvents. Suitable combination of flexible/rigid segments in molecular spacers in the present cholesteryl gelators is favorable for the gelation of organic solvents. Morphological studies revealed that the gelator molecules self-assemble into different aggregates, from wrinkle and belt to fiber with Blasticidin S ic50 the change of spacers and solvents.
Spectral studies indicated that there existed different H-bond formations between imide groups and assembly modes, depending on the substituent spacers in molecular skeletons. The prepared nanostructures have wide perspectives and many potential applications
in nanoscience and material fields due to their scientific values. These results afford useful Epoxomicin clinical trial information for the design and development of new versatile low molecular mass organogelators and soft matter. Authors’ information TJ and QZ are associate professors. FeG is an MD student. FaG is a professor and the Dean of the School of Environmental and Chemical Engineering. JZ is a laboratory assistant in Yanshan University. Acknowledgements This work was financially supported by the National Natural Science Foundation of China (grant no. 21207112), the Natural Science Foundation of Hebei Province (grant nos. B2012203060 and B2013203108), the China Postdoctoral Science Foundation (grant nos. 2011M500540, 2012M510770, and 2013T60265), the Science Foundation for the Excellent Youth Scholars from Universities and Colleges of Hebei Province (grant nos. Y2011113 and YQ2013026), the Scientific Research Foundation for Returned Overseas Chinese Scholars of Hebei
Alectinib clinical trial Province (grant no. 2011052), and the Open Foundation of State Key Laboratory of Solid Lubrication (Lanzhou Institute of Chemical Physics, CAS; grant no. 1002). References 1. Su YS, Liu JW, Jiang Y, Chen CF: Assembly of a self-complementary monomer: formation of supramolecular polymer networks and responsive gels. Chem Eur J 2011, 17:2435–2441.CrossRef 2. Li J, Kuang Y, Gao Y, Du X, Shi J, Xu B: d-Amino acids boost the selectivity and confer supramolecular hydrogels of a nonsteroidal anti-inflammatory drug (NSAID). J Am Chem Soc 2013, 135:542–545.CrossRef 3. Oh H, Jung BM, Lee HP, Chang JY: Dispersion of single walled carbon nanotubes in organogels by incorporation into organogel fibers. J Colloid Interf Sci 2010, 352:121–127.CrossRef 4. Delbecq F, Tsujimoto K, Ogue Y, Endo H, Kawai T: N-stearoyl amino acid derivatives: Pritelivir supplier potent biomimetic hydro/organogelators as templates for preparation of gold nanoparticles. J Colloid Interf Sci 2013, 390:17–24.CrossRef 5. Liu JW, Yang Y, Chen CF, Ma JT: Novel anion-tuning supramolecular gels with dual-channel response: reversible sol–gel transition and color changes. Langmuir 2010, 26:9040–9044.CrossRef 6.