Add time:09/28/2019         Source:infona.pl

Four heterocyclic salts 1a–d were prepared by Ca 2+ -assisted cyclization of fluoro derivatives 3, and investigated by spectroscopic (NMR and UV), electrochemical, and computational (DFT and MP2) methods. The mechanism for the formation of the cations was investigated at the DFT level of theory. 2-D NMR spectroscopy for 1[ClO 4 ] in DMSO­d 6 aided with DFT results permitted the assignment of 1 H and 13 C NMR signals in cations 1. The molecular and crystal structures for 1a[ClO 4 ] [C 13 H 10 ClNO 4 triclinic, P−1, a=9.6517(12) Å, b=11.0470(13) Å, c=12.2373(15) Å, α=67.615(1)°, β=78.845(2)°, γ=87.559(2)°; V=1183.0(2) Å 3 , Z=4] and 1d[ClO 4 ] [C 12 H 9 ClN 2 O 4 triclinic, P−1, a=5.9525(6) Å, b=8.3141(9) Å, c=12.2591(13) Å, α=73.487(1)°, β=83.814(1)°, γ=83.456(1)°; V=576.07(10) Å 3 , Z=2] were determined by X-ray crystallography and compared with results of DFT and MP2 calculations. Electrochemical analysis gave the reduction potential order (1b>1c∼1d>1a), which is consistent with computational results.

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