Paper Info
Title
A Computational Study Of Unique Properties Of Pillar[N]Quinones: Self-Assembly To Tubular Structures And Potential Applications As Electron Acceptors And Anion Recognizers
Abstract
Density functional theory has been used to calculate the thermodynamic properties and molecular orbitals of pillar[n]quinones. Pillar[n]quinones are expected to be effective electron acceptors and the ability to accept more than one electron increases with the size of the interior cavity. Pillar[5]quinone and pillar[7]quinone show a great intramolecular charge transfer upon the electron excitation from highest occupied molecular orbital (HOMO) to lowest unoccupied molecular orbital (LUMO) as indicated by a large difference of electron distributions between their HOMO and LUMO and a notable dipole moment difference between the ground and first triplet excited state. The aggregation of pillar[n]quinones leads to tubular dimeric structures joined by 2n C-H center dot center dot center dot O nonclassical hydrogen bonds (HBs) with binding energies about 2 kcal/mol per HB. The longitudinal extension of the supramolecular self-assembly of pillar[n]quinone may be adjustable through forming and breaking their HBs by controlling the surrounding environment. The tunability of the diameter of the tubular structures can be achieved by changing the number of quinone units in the pillar[n]quinone. The electrostatic potential maps of pillar[n]quinones indicate that the positive charge in the interior cavity decreases as the number of quinone units increases. Chloride and bromide anions are chosen to examine the noncovalent anion-pi interactions between pillar[n]quinones and captured anions. The calculations show that the better compatibility of the effective radius of the anions with the interior dimension of pillar[n]quinone leads to larger stabilization energy. The selectivity of spatial matching and specific interaction of pillar[n]quinone is believed to possibly serve as a candidate for ionic and molecular recognition. (C) 2011 Wiley Periodicals, Inc. J Comput Chem 32: 2716-2726, 2011
Year
DOI
Venue
2011
10.1002/jcc.21853
JOURNAL OF COMPUTATIONAL CHEMISTRY
Keywords
Field
DocType
para-bridged macrocyclic molecule, tubular structures, selfassembly, anion-pi, interactions, density functional theory
Ionic bonding,Molecular orbital,Excited state,Electron acceptor,Quinone,Computational chemistry,Chemistry,Density functional theory,HOMO/LUMO,Supramolecular chemistry
Journal
Volume
Issue
ISSN
32
12
0192-8651
Citations 
PageRank 
References 
0
0.34
0
Authors
2
Name
Order
Citations
PageRank
Ka-Un Lao100.34
Chin-hui Yu231.93