Journal
JOURNAL OF ORGANIC CHEMISTRY
Volume 88, Issue 6, Pages 3466-3473Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.joc.2c025203466J
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Four isomeric dithienoporphyrins (2.1.2.1) were synthesized using two di(1H-pyrrolo-2-yl)thiophenes and two arylaldehydes under mild acid-catalyzed conditions. The dithienoporphyrins (2.1.2.1) exhibited altered molecular geometry and optical and electronic properties compared to other dibenzo-/dinaphthopor-phyrins(2.1.2.1). These dithienoporphyrins(2.1.2.1) can form metal complexes with nickel(II), copper(II), and palladium(II) ions, which exhibit bent molecular conformations and are influenced by the inserted metal ions.
Four kinds of isomeric dithienoporphyrins(2.1.2.1) were prepared using two di(1H-pyrrolo-2-yl)thiophenes as building blocks and two arylaldehydes under mild acid-catalyzed conditions. The molecular conformation and optical and electronic properties of dithienoporphyrins(2.1.2.1) were investigated by NMR spec-troscopy, X-ray diffraction, UV-vis absorption spectroscopy, electrochemical measurements, and theoretical calculations. The crystal structure of [2,3]F5TP has the largest angle between the two planes of the dipyrrin units among dibenzo-/dinaphthopor-phyrins(2.1.2.1). This result indicates that the incorporation of thiophene subunits into a porphyrin(2.1.2.1) macrocycle results in the alteration of the molecular geometry to a more planarized structure. Dithienoporphyrin(2.1.2.1) is found to act as a ligand that can form metal complexes with nickel(II), copper(II), and palladium(II) ions. The molecular structures of the dithienoporphyrin(2.1.2.1) metal complexes exhibited bent molecular conformations. The red-shifted absorption, reversible redox processes, and theoretical calculations indicated that the electronic properties of the dithienoporphyrin(2.1.2.1) metal complexes are controlled by the inserted metal ions.
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