Details of the intermolecular interactions in poly(vinyl alcohol)-iodine complexes as studied by quantum chemical calculations. (2nd September 2016)

• Record Type: Journal Article
• Authors: Takahama, Tomohiko; Saharin, Siti Munirah; Tashiro, Kohji
• Is Part Of: Polymer. Volume 99(2016)
• Page Start: 566
• Page End: 579
• Publication Date: 2016-09-02
• Subjects: Poly(vinyl alcohol) -- Iodine complex -- Intermolecular interaction -- Quantum chemical calculations; Polymers -- Periodicals; Polymerization -- Periodicals; Polymères -- Périodiques; Polymérisation -- Périodiques; 547.7
• DOI: 10.1016/j.polymer.2016.07.055
• Languages: English
• ISSNs: 0032-3861

Abstract

Abstract: The electronic state of poly(vinyl alcohol) (PVA)-I3 − ion complex has been successfully described for the first time on the basis of the density functional theoretical (DFT) calculations. (1) As the first trial, complex structure models between a short PVA chain (5-mer) and I3 − ion were constructed, which were geometrically optimized and the energy change during the complexation was analyzed. Mainly the interaction between OH groups of PVA and iodine has been found to determine the stability of the complex. The interaction strength depends on the stereoregularity of the chain: the syndiotactic PVA sequence gave the strongest interactions between I3 − and four or five OH sequence along the chain axis, while the atactic and isotactic chain models are less stable than the former case. The calculated interaction energy between PVA and I3 − species was 36.0, 31.2 and 25.6 kcal/mol for syndiotactic, atactic and isotactic PVA, respectively. The calculation of orbital interactions revealed that the highest occupied molecular orbital (HOMO) of I3 − is relatively close to the lowest unoccupied MO (LUMO) of PVA, causing an electron transfer from I3 − to PVA. (2) In the second-stage calculation, the crystal structure model of PVA-iodine complex including counter ions (K + ) was built up by referring to the X-ray analyzed structure. The K + ions were found to be localized in the highly-negatively-charged space surrounded by OH groups and iodine atoms, corresponding well to the electrostatic potential minimum created by the PVA chains and iodine ions. The local molecular orbitals (LMO) calculated for these two models [(1) and (2)] revealed the existence of H-bonding interaction between the OH group and the iodine ion. Graphical abstract: Highlights: Intermolecular interactions and crystal structure of PVA－I3 － complex were studied by DFT. OH⋯I type hydrogen bonds are the main interaction to induce the complexation. Syndiotactic sequence of PVA chain gave the strongest interactions with iodine ions. DFT-optimized crystal structure of the complex fitted well the X-ray analyzed structure. K + ions, not identified by X-ray analysis, were found to locate near the electrostatic potential minimum.