RT Book,_Section
T1 Synthesis and Characterization of a New Triptycene-Based Tripod
A1 Sanmartín Matalobos, Jesús
A1 García Deibe, Ana María
A1 Fondo Busto, María Matilde
A1 Pérez Lustres, José Luis
A1 Bhowmick, Sourav
A1 Das, Neeladri
K1 Fluorescence emission
K1 Triptycene derivatives
K1 Schiff bases
K1 Tripods
AB Herein, we report an efficient and facile synthesis of a new triptycene based tripodal ligand containing both imine functionality and phenolic pendant arms. This tripodal unit is a potential building block for constructing novel supramolecular architectures. The newly synthesized 2,6,14-triaminotriptycene derivative, which was characterized by FT-IR, UV−Vis absorption, mass and NMR spectroscopic techniques has interesting properties such as high solubility in common organic solvents and fluorescence emission in THF solution (λ = 550 nm)
PB MDPI
SN 978-3-906980-55-3
YR 2015
FD 2015
LK http://hdl.handle.net/10347/25971
UL http://hdl.handle.net/10347/25971
LA eng
NO Sanmartín-Matalobos, J., García-Deibe, A., Fondo, M., Pérez-Lustres, J.L., Bhowmick, S. & Das, N. (2015). Synthesis and Characterization of a New Triptycene-Based Tripod. In J.A. Seijas, M.P. Vázquez Tato & S.K. Lin, Proceedings ECSOC-18: The 18Th International Electronic Conference On Synthetic Organic Chemistry: November 1-30, 2014. MDPI. doi: 10.3390/ecsoc-18-a007
NO The 18th International Electronic Conference on Synthetic Organic Chemistry session General Organic Synthesis
DS Minerva
RD 23 abr 2026