TY - JOUR
T1 - Revisiting Pentazole
T2 - An Investigation into the Intriguing Molecule Exhibiting Dual Organic and Inorganic Characteristics
AU - Xia, Honglei
AU - Jiang, Tianyu
AU - Qi, Guangyu
AU - Liu, Tianlin
AU - Zhang, Wenquan
AU - Zhang, Qinghua
N1 - Publisher Copyright:
© 2024 American Chemical Society.
PY - 2024/7/22
Y1 - 2024/7/22
N2 - Pentazole (cyclo-HN5) is a unique heterocycle categorized as both an organic and inorganic compound. However, attempts to synthesize and characterize cyclo-HN5 have been unsuccessful thus far. In this study, we synthesized a cyclo-HN5 solution and investigated the spectra, structure, aromaticity, acidity, and stability of cyclo-HN5. The lone pair of electrons on the protonated N atom of cyclo-HN5 participates in π-electron delocalization, forming two N═N bonds. Further investigations suggest that cyclo-HN5 exhibits significantly decreased π aromaticity and slightly lower σ aromaticity than cyclo-N5-. Experimental results suggest that pure cyclo-HN5 is unstable at ambient temperatures and pressures, but it can be isolated at high pressures or stabilized in solution by abundant hydrogen bonds. The pKa of cyclo-HN5 was determined as 1.63 (H2O, 25 °C) via potentiometric titration, indicating that cyclo-HN5 is a medium-strong acid. This study reveals the fundamental structure and properties of cyclo-HN5, thereby providing important data for advancing cyclo-HN5 chemistry.
AB - Pentazole (cyclo-HN5) is a unique heterocycle categorized as both an organic and inorganic compound. However, attempts to synthesize and characterize cyclo-HN5 have been unsuccessful thus far. In this study, we synthesized a cyclo-HN5 solution and investigated the spectra, structure, aromaticity, acidity, and stability of cyclo-HN5. The lone pair of electrons on the protonated N atom of cyclo-HN5 participates in π-electron delocalization, forming two N═N bonds. Further investigations suggest that cyclo-HN5 exhibits significantly decreased π aromaticity and slightly lower σ aromaticity than cyclo-N5-. Experimental results suggest that pure cyclo-HN5 is unstable at ambient temperatures and pressures, but it can be isolated at high pressures or stabilized in solution by abundant hydrogen bonds. The pKa of cyclo-HN5 was determined as 1.63 (H2O, 25 °C) via potentiometric titration, indicating that cyclo-HN5 is a medium-strong acid. This study reveals the fundamental structure and properties of cyclo-HN5, thereby providing important data for advancing cyclo-HN5 chemistry.
UR - http://www.scopus.com/inward/record.url?scp=85199184545&partnerID=8YFLogxK
U2 - 10.1021/acs.inorgchem.4c01050
DO - 10.1021/acs.inorgchem.4c01050
M3 - 文章
C2 - 38973778
AN - SCOPUS:85199184545
SN - 0020-1669
VL - 63
SP - 13166
EP - 13170
JO - Inorganic Chemistry
JF - Inorganic Chemistry
IS - 29
ER -