Measurement of Solvation Ability of Solvents by Porphyrin-Based Solvation/Desolvation Indicators

被引:7
作者
Sugimoto, Motonobu [1 ]
Kuramochi, Yusuke [1 ]
Satake, Akiharu [1 ]
机构
[1] Tokyo Univ Sci, Grad Sch Sci, Shinjuku Ku, Tokyo 1628601, Japan
关键词
AROMATIC RINGS; STACKING; MACROCYCLES; BENZENE;
D O I
10.1021/acsomega.9b04461
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A new solvent scale, solvation ability (SA), was developed to arrange solvents in the order of their SA for large pi-conjugated compounds. The SA of a solvent was determined in a binary solvent system of an assessed solvent and a standard "good" solvent (GS) or "poor" solvent (PS), chloroform or methylcyclohexane, respectively, in the presence of two types of solvation/desolvation indicators, 1Zn(2) and 2Zn(2). The latter comprises bis(imidazolylporphyrinatozinc) linked via a 1,3-butadiynylene moiety having linear alkyl and hydrophilic side chains, respectively. GSs and PSs give extended (E-) and stacked (S-) supramolecular polymers of the indicators, respectively. SA values are defined as vol % of the standard solvent added to an assessed solvent to give the balance point where comparable amounts of E- and S-polymers of the indicators coexist. GSs and PSs have positive and negative signs, respectively. In this study, the SA of 25 solvents was determined. The SA values with indicator 1Zn(2) were as follows: ethyl acetate (-81), hexane (-50), cyclohexane (-47), CCl4 (-25), chloroform (50), and nitrobenzene (79).
引用
收藏
页码:6045 / 6050
页数:6
相关论文
共 34 条
[1]   A rigid molecular balance for measuring face-to-face arene-arene interactions [J].
Carroll, William R. ;
Pellechia, Perry ;
Shimizu, Ken D. .
ORGANIC LETTERS, 2008, 10 (16) :3547-3550
[2]   Solvent and substituent effects on aggregation constants of perylene bisimide π-stacks - a linear free energy relationship analysis [J].
Chen, Zhijian ;
Fimmel, Benjamin ;
Wuerthner, Frank .
ORGANIC & BIOMOLECULAR CHEMISTRY, 2012, 10 (30) :5845-5855
[3]   Self-assembled π-stacks of functional dyes in solution: structural and thermodynamic features [J].
Chen, Zhijian ;
Lohr, Andreas ;
Saha-Moeller, Chantu R. ;
Wuerthner, Frank .
CHEMICAL SOCIETY REVIEWS, 2009, 38 (02) :564-584
[4]   Substituent effects on aromatic stacking interactions [J].
Cockroft, Scott L. ;
Perkins, Julie ;
Zonta, Cristiano ;
Adams, Harry ;
Spey, Sharon E. ;
Low, Caroline M. R. ;
Vinter, Jeremy G. ;
Lawson, Kevin R. ;
Urch, Christopher J. ;
Hunter, Christopher A. .
ORGANIC & BIOMOLECULAR CHEMISTRY, 2007, 5 (07) :1062-1080
[5]   1H NMR investigation of solvent effects in aromatic stacking interactions [J].
Cubberley, MS ;
Iverson, BL .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2001, 123 (31) :7560-7563
[6]  
DIMROTH K, 1963, LIEBIGS ANN CHEM, V661, P1
[7]   Cation-pi interactions in chemistry and biology: A new view of benzene, Phe, Tyr, and Trp [J].
Dougherty, DA .
SCIENCE, 1996, 271 (5246) :163-168
[8]  
Fukui T, 2017, NAT CHEM, V9, P493, DOI [10.1038/nchem.2684, 10.1038/NCHEM.2684]
[9]   Solvent-dependent stabilization of the E configuration of propargylic secondary amides [J].
Gardner, RR ;
McKay, SL ;
Gellman, SH .
ORGANIC LETTERS, 2000, 2 (15) :2335-2338
[10]   THE NATURE OF PI-PI INTERACTIONS [J].
HUNTER, CA ;
SANDERS, JKM .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1990, 112 (14) :5525-5534