Jump to main content
Jump to site search
PLANNED MAINTENANCE Close the message box

Scheduled maintenance upgrade on Thursday 4th of May 2017 from 8.00am to 9.00am (BST).

During this time our websites will be offline temporarily. If you have any questions please use the feedback button on this page. We apologise for any inconvenience this might cause and thank you for your patience.

Electronic Structure and Conformational Conversion of Calix[4]arene Complexes with Alkali Metal Ions


Ultraviolet photodissociation (UVPD) spectra of calix[4]arene (C4A) complexes with alkali metal ions, M+•C4A (M = Na, K, Rb, and Cs), are measured in the 34000–37000 cm-1 region under cold (~10 K) conditions in the gas phase. The Na+•C4A and K+•C4A complexes show several sharp vibronic bands, while the UVPD spectra of the Rb+•C4A and Cs+•C4A complexes exhibit only broad features. The UVPD spectra are assigned with the aid of quantum chemical calculations. Most of the features in the UVPD spectra can be attributed to cone isomers, which are the most stable for all the M+•C4A complexes. In all the cone isomers, the M+ ion is encapsulated inside the cavity of C4A, and the structure is distorted to C2 symmetry from that of bare C4A (C4 symmetry). The cone isomers show a substantial difference in the electronic structure between the K+ and Rb+ complexes. The Rb+ and Cs+ complexes have an electronic structure similar to that of bare C4A. In the Na+ and K+ complexes, a pair of two benzene rings facing to each other has a short distance between them (< 6 Å). This results in substantial overlap of π clouds between them, and an electronic transition is localized on this pair. Only this localized electronic transition of the Na+ and K+ complexes shows sharp band features in the UVPD spectra. In the Na+•C4A complex, the UVPD spectroscopic result suggests the coexistence of other isomers having a partial cone and 1,3-alternate form. The energetics for isomerization reactions of C4A and Na+•C4A is examined theoretically. Estimated potential barriers between the stable conformers are less than 75 kJ/mol for Na+•C4A, suggesting that conformational conversion can occur at room temperature, before the Na+•C4A complex enters the cold ion trap. The existence of multiple conformations for Na+•C4A is attributed to higher stability of these conformers, both kinetically and thermodynamically, compared to the case of bare C4A and the other M+•C4A complexes.

Back to tab navigation
Please wait while Download options loads

Supplementary files

Publication details

The article was received on 12 Mar 2017, accepted on 12 Apr 2017 and first published on 19 Apr 2017

Article type: Paper
DOI: 10.1039/C7CP01580A
Citation: Phys. Chem. Chem. Phys., 2017, Accepted Manuscript
  •   Request permissions

    Electronic Structure and Conformational Conversion of Calix[4]arene Complexes with Alkali Metal Ions

    Y. Inokuchi, K. Hirai and T. Ebata, Phys. Chem. Chem. Phys., 2017, Accepted Manuscript , DOI: 10.1039/C7CP01580A

Search articles by author