First Sublimation Thermodynamics and First Gas‐Phase Experimental Molecular Structure of Heteroporphyrins: 5,10,15,20‐Tetraphenyl‐21‐X, 23‐Y‐Porphyrins (X=O or S; Y=N or S)

Abstract

First sublimation enthalpies of heteroporphyrins: 10,15,20‐tetraphenyl‐21‐oxa‐ (HOPP), 5,10,15,20‐tetraphenyl‐21‐thia‐ (HSPP) and 5,10,15,20‐tetraphenyl‐21,23‐dithia‐ (S2PP) were measured by Knudsen effusion mass spectrometry: ΔsublH (T)=209±2 (561 K), 224±2 (552 K) and 219±2 (577 K) kJ/mol, respectively. Geometry and force field of a free molecule of HSPP was studied by quantum chemistry, and first gas‐phase experimental molecular structure of heteroporphyrins was derived by gas‐phase electron diffraction. Theoretically observed changes of the coordination cavity geometries due to heteroatomic intracavity substitution were experimentally confirmed with good agreement. Molecular structures of the dimeric associates of the heteroporphyrins were tested simulated to reveal tendencies in sublimation thermodynamics.