1 research outputs found
Synthesis of 21,23-Selenium- and Tellurium-Substituted 5‑Porphomethenes, 5,10-Porphodimethenes, 5,15-Porphodimethenes, and Porphotrimethenes and Their Interactions with Mercury
The 3+1 condensation of symmetrical
16-Selena/telluratripyrranes
with symmetrical selenophene-2,5-diols/tellurophene-2,5-diols in the
presence of BF<sub>3</sub>-etheratre or BF<sub>3</sub>-methanol followed
by oxidation with DDQ gave 5,10-porphodimethenes, whereas the process
with unsymmetrical selenophene-2,5-diols/tellurophene-2,5-diols gave
5-porphomethenes. In addition, the reaction of unsymmetrical 16-Selena/telluratripyrranes
with symmetrical selenophene-2,5-diols/tellurophene-2,5-diols gave
the corresponding porphotrimethenes, whereas the process with unsymmetrical
selenophene-2,5-diols/tellurophene-2,5-diols gave the 5,15-porphodimethenes.
The structures of different products were characterized by IR, <sup>1</sup>H and <sup>13</sup>C NMR, <sup>1</sup>H–<sup>1</sup>H COSY, CHN analysis, and mass spectrometry. The binding of mercury
with the calix[4]Âphyrins mentioned above had been observed in the
decreasing order of porphodimethenes > porphomethenes > porphotrimethenes
by UV–vis and <sup>1</sup>H NMR spectroscopy