107975-90-6Relevant academic research and scientific papers
Design of Novel Mesomorphic Compounds: N,N',N"-Trialkyl-1,3,5-benzenetricarboxamides
Matsunaga, Yoshio,Miyajima, Nobuhiko,Nakayasu, Yuichi,Sakai, Satoshi,Yonenaga, Michihiro
, p. 207 - 210 (1988)
N,N'-Dialkyl-1,4-benzenedicarboxamides melt with anomalously small enthalpy changes.The 1,3-analogs behave similarly but at lower temperatures.These observations provide a clue to design novel mesomorphic compounds; N,N',N''-trialkyl-1,3,5-benzenetricarbo
Synthesis and NMR Spectroscopic Study of the Self-Aggregation of 2-Substituted Benzene-1,3,5-tricarboxamides
Invernizzi, Christian,Dalvit, Claudio,Stoeckli-Evans, Helen,Neier, Reinhard
, p. 5115 - 5127 (2015/08/18)
The self-assembly of N,N′,N′-trialkylbenzene-1,3,5-tricarboxamides (BTAs) 1 or of "crowded" BTAs 11 and 12 lead to supramolecular columnar-stacked structures with attractive material properties. The introduction of three alkoxy groups is reported to reinf
Phase behavior and mesophase structures of 1,3,5-benzene- and 1,3,5-cyclohexanetricarboxamides: Towards an understanding of the losing order at the transition into the isotropic phase
Timme, Andreas,Kress, Roman,Albuquerque, Rodrigo Q.,Schmidt, Hans-Werner
supporting information; experimental part, p. 8329 - 8339 (2012/08/07)
One of the simplest and most-versatile motifs in supramolecular chemistry is based on 1,3,5-benzenetricarboxamides. Variation of the core structure and subtle changes in the structures of the lateral substituents govern the self-assembly and determine the
Antimicrobial effects of oligoamines
Rehse, Klaus,Woyke, Christian,Rodloff, Arne,Hahn, Helmut
, p. 155 - 160 (2007/10/03)
Twenty-four oligoamines belonging to six (1-6) structurally different types were tested in vitro for the antibacterial activity against 14 different bacterial species comprising a total of 187 strains. Ten compounds were able to inhibit growth of at least
