Glass-forming Schiff bases: Peculiar self-organizing systems with bifurcated hydrogen bonds

被引:2
作者
Nowok, Andrzej [1 ]
Cieslik, Wioleta [2 ]
Dulski, Mateusz [3 ,4 ]
Jurkiewicz, Karolina [1 ,3 ]
Grelska, Joanna [1 ,3 ]
Aleman, Jose [5 ,6 ]
Musiol, Robert [2 ]
Szeremeta, Anna Z. [1 ]
Pawlus, Sebastian [1 ,3 ]
机构
[1] Univ Silesia Katowice, August Chelkowski Inst Phys, 75 Pulku Piechoty 1, PL-41500 Chorzow, Poland
[2] Univ Silesia Katowice, Inst Chem, 75 Pulku Piechoty 1A, PL-41500 Chorzow, Poland
[3] Silesian Ctr Educ & Interdisciplinary Res, 75 Pulku Piechoty 1A, PL-41500 Chorzow, Poland
[4] Univ Silesia Katowice, Inst Mat Engn, 75 Pulku Piechoty 1A, PL-41500 Chorzow, Poland
[5] Univ Autonoma Madrid, Dept Organ Chem, Calle Francisco Tomas y Valiente, Madrid 28049, Spain
[6] Univ Autonoma Madrid, Inst Adv Res Chem Sci IAdChem, Madrid 28049, Spain
关键词
Schiff base; Glass transition; Bifurcated hydrogen bonds; Self-assembly; Molecular dynamics; SLOW SECONDARY RELAXATION; FEMTOSECOND FLUORESCENCE; CONJUGATE ADDITION; CRYSTAL-STRUCTURE; PROTON-TRANSFER; COMPLEXES; VISCOSITY; DYNAMICS; MODEL; WATER;
D O I
10.1016/j.molliq.2021.118052
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A combination of quantum computations with calorimetric, dielectric, infrared, and diffraction studies was used to dissect the nature of atypical bifurcated (three-centered) hydrogen bonds (BHBs). Based on the analysis of four glass-forming Schiff bases, this article experimentally proves that self-organization via BHBs may be prevalent in H-bonding systems. Moreover, it explicitly shows that even high screening of the proton-donor and proton-acceptor groups is not a sufficient obstacle to form the BHBs. Even highly sterically hindered Schiff bases form lasting centrosymmetric dimers via a pair of BHBs in the liquid and glass phases. The driving force for their medium-range-scale ordering tendency is a disorder in the molecular scaffold, strictly bound to the N center dot center dot center dot H center dot center dot center dot O bond character. As a result, the protons of the BHBs center gain translational freedom. Finally, it is shown that, contrary to the prevailing opinion, Schiff bases can be good glass-forming systems with high glass transition temperatures. (C) 2021 Elsevier B.V. All rights reserved.
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页数:8
相关论文
共 52 条
[21]   AN ELECTROSTATIC MODEL FOR HYDROGEN-BONDS IN ALCOHOLS [J].
GIGUERE, PA ;
PIGEONGOSSELIN, M .
JOURNAL OF SOLUTION CHEMISTRY, 1988, 17 (11) :1007-1014
[22]   THE BIFURCATED HYDROGEN-BOND MODEL OF WATER AND AMORPHOUS ICE [J].
GIGUERE, PA .
JOURNAL OF CHEMICAL PHYSICS, 1987, 87 (08) :4835-4839
[23]   BIFURCATED HYDROGEN-BONDS IN WATER [J].
GIGUERE, PA .
JOURNAL OF RAMAN SPECTROSCOPY, 1984, 15 (05) :354-359
[24]   2-Hydroxybenzophenone as a Chemical Auxiliary for the Activation of Ketiminoesters for Highly Enantioselective Addition to Nitroalkenes under Bifunctional Catalysis [J].
Guerrero-Corella, Andrea ;
Esteban, Francisco ;
Iniesta, Manuel ;
Martin-Somer, Ana ;
Parra, Mario ;
Diaz-Tendero, Sergio ;
Fraile, Alberto ;
Aleman, Jose .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2018, 57 (19) :5350-5354
[25]   A COMPLEX PLANE REPRESENTATION OF DIELECTRIC AND MECHANICAL RELAXATION PROCESSES IN SOME POLYMERS [J].
HAVRILIA.S ;
NEGAMI, S .
POLYMER, 1967, 8 (04) :161-&
[26]  
Hehre W., 1986, Ab Initio Molecular Orbital Theory
[27]  
Hossain S.M., 2018, International Journal of Chemical Research, V6, P19
[28]   Silver/ThioClickFerrophos-Catalyzed Enantioselective Conjugate Addition and Cycloaddition of Glycine Imino Ester with Nitroalkenes [J].
Imae, Kazumi ;
Konno, Takashi ;
Ogata, Kenichi ;
Fukuzawa, Shin-ichi .
ORGANIC LETTERS, 2012, 14 (17) :4410-4413
[29]   Review on Schiff bases and their metal complexes as organic photovoltaic materials [J].
Jeevadason, A. Wesley ;
Murugavel, K. Kalidasa ;
Neelakantan, M. A. .
RENEWABLE & SUSTAINABLE ENERGY REVIEWS, 2014, 36 :220-227
[30]   3-CENTER (BIFURCATED) HYDROGEN-BONDING IN THE CRYSTAL-STRUCTURES OF AMINO-ACIDS [J].
JEFFREY, GA ;
MITRA, J .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1984, 106 (19) :5546-5553