Studies have revealed how pressure influences the path of one photochemical reaction in crystals. The single-crystal-to-single-crystal Norrish–Yang reaction of 4-(2,4,6-triisopropylbenzoyl)benzoate benzylammonium, compound 1, was studied at high pressures of 0.3 and 0.9 GPa. X-ray structure analysis was used in order to monitor the kinetics of the reaction and the structural changes induced by UV radiation and pressure. The reaction rate is lower at higher pressure: the rate constants are 5.3 × 10⁻⁵ s⁻¹ and 4.3 × 10⁻⁶ s⁻¹ at 0.3 and 0.9 GPa, respectively. This was rationalized by: (a) the decrease in the size of voids near the reaction centre and in the unit cell with pressure, (b) the increase of intermolecular interactions in which the photoreactive o-isopropyl group takes part along with pressure and (c) the structural changes brought about by the photochemical reaction itself, for example, the increase of the unit cell volume. Pressure significantly reduced these structural changes and even halted some of them.

The present work describes the preparation and characterization of a new cobalt(III) porphyrin coordination compound named (chlorido)(nicotinoylchloride)[meso-tetra(para-chlorophenyl)porphyrinato]cobalt(III) dichloromethane monosolvate with the formula [Co^III(TClPP)Cl(NTC)]·CH₂Cl₂ (4). The single-crystal X-ray molecular structure of 4 shows very important ruffling and waving distortions of the porphyrin macrocycle. The Soret and Q absorption bands of 4 are very red-shifted as a consequence of the very distorted porphyrin core. This coordination compound was also studied by fluorescence and cyclic voltammetry. The efficiency of our four porphyrinic compounds—the H₂TClPP (1) free-base porphyrin, the [Co^II(TClPP)] (2) and [Co^III(TClPP)Cl] (3) starting materials, and the new Co(III) metalloporphyrin [Co^III(TClPP)Cl(NTC)]·CH₂Cl₂ (4)—as catalysts in the photochemical degradation was tested on malachite green (MG) dye. The current voltage of complexes 3 and 4 was also studied. Electrical parameters, including the saturation current density (J_s) and barrier height (ϕ_b), were measured.

The [2 + 2] photodimerization of 2,6-difluorocinnamic acid was gradually induced in crystals by UV radiation at 0.5, 1.1 and 2.1 GPa. The crystal and molecular structures were determined before the photochemical reaction and for many of its steps. For the pure monomer structures, the following parameters were analyzed in order to gain knowledge of the influence of pressure on the reaction environment: (a) the volume of free space, (b) the geometry of close intermolecular interactions, including hydrogen bonds and (c) the geometry of intermolecular reactivity parameters. The following structural changes brought about by the [2 + 2] photodimerization at high pressure were monitored step-by-step: (a) the cell parameters and the cell volume, (b) the content of the monomer and the dimer, (c) the distance between the reactive carbon atoms in adjacent monomer molecules and (d) the geometry of mutual orientation of molecules in the crystals. The rate of the [2 + 2] photodimerization of 2,6-difluorocinnamic acid increased as follows: 0.1 MPa < 0.5 GPa < 1.1 GPa ≤ 2.1 GPa. This was rationalized by the decrease in the volume of free space columns protecting the intermolecular geometry suitable for the reaction and by the decrease of the distance between the reactive carbon atoms of adjacent monomer molecules.