2402-58-6Relevant articles and documents
Face-to-Face Packing of 2,3,9,10-Tetrasubstituted Pentacene Derivatives Revealed through a Solid State [4 + 4] Thermal Cycloaddition and Molecular Dynamic Simulation
Pal, Bikash,Lin, Bo-Chao,Dela Cerna, Mark Vincent Carreon,Hsu, Chao-Ping,Lin, Chih-Hsiu
, p. 6223 - 6234 (2016/08/16)
2,3,9,10-Substituted pentacene tetraesters and pentacene diester-dinitriles were synthesized. These pentacene derivatives underwent an unusual solid state [4 + 4] thermal dimerization with good efficiency and complete stereoselectivity. This observation indicates this series of pentacene derivatives adopt π-π stacking geometry with large mutual overlap in solid state. This notion was confirmed by molecualr dynamic simulation.
trans-2-Aminocyclohexanol as a pH-sensitive conformational switch in lipid amphiphiles
Brazdova, Barbora,Zhang, Ningrong,Samoshin, Vyacheslav V.,Guo, Xin
supporting information; experimental part, p. 4774 - 4776 (2009/03/12)
Protonation-induced conformational change of lipid tails is reported as a novel strategy to render pH-sensitive lipid amphiphiles and lipid colloids. The Royal Society of Chemistry.
