3,6,13,16-Tetrapropylporphycene: Rational Synthesis, Complexation, and Halogenation
作者:Jodukathula Nagamaiah、Arnab Dutta、Narendra Nath Pati、Sameeta Sahoo、Rahul Soman、Pradeepta K. Panda
DOI:10.1021/acs.joc.1c02652
日期:2022.3.4
time as its alkyl analogue fromethyl 4-propyl-1H-pyrrole-2-carboxylate. The substituent effect was found to be more intense than reported positional isomeric tetrapropylporphycenes. The freebase porphycene exhibited moderate fluorescence and complexation ability with divalent metal ions, including Zn(II), which displayed an enhanced emission quantum yield (∼30%). The Pd(II) complex and freebase β-tetrabromoporphycene