Wydział Chemii

Krystyna Rachlewicz

Natasza Sprutta

Piotr J. Chmielewski

Lechosław Latos-Grażyński

1998

Journal of the Chemical Society-Perkin Transactions 2: Physical Organic Chemistry

969-975

10.1039/A705496C

Naukowa

Angielski

Artykuł

5,10,15,20-Tetraphenyl-26,28-dioxasapphyrin (O₂TPSH) and 5,10,15,20-tetraphenyl-26,28-dithiasapphyrin (S₂TPSH), heteroanalogues of 5,10,15,20-tetraphenylsapphyrin (TPSH₃) have been synthesised by condensation of the respective precursors, namely 2,5-bis(arylhydroxymethyl)furan or bis(arylhydroxymethyl)thiophene and pyrrole. 26,28-Dioxasapphyrin presents an unusual skeleton with an inverted pyrrole ring lying opposite to the bipyrrolic unit at each protonation stage. In contrast, the planar arrangement of the macrocycle has been determined for 26,28-dithiasapphyrin.The tautomeric equilibrium of S₂TPSH which involves the exchange of a proton between N-25 and N-29 has been found to be slow on the ¹H NMR timescale below 213 K. Activation parameters of tautomerization were determined by the line shape analysis: ΔH ^‡ = 47.2 ± 1.1 kJ mol^–1, ΔS ^‡ = 19.9 ± 5.5 J K^–1 (ΔH ^‡ = 10.9 ± 0.3 kcal mol^–1, ΔS ^‡ = 4.6 ± 1.4 cal K^–1).

DOI https://doi.org/10.1039/A705496C

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