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1H and 13C NMR assignments for new heterocyclic TAM leuco dyes, (2Z,2′E)-2,2′-(2-phenyl propane-1,3-diylidene) bis(1,3,3-trimethylindoline) derivatives.: Part II
被引:10
|作者:
Keum, Sam-Rok
[1
]
Roh, Se-Jung
[1
]
Lee, Min-Hyung
[1
]
Sauriol, Francoise
[2
]
Buncel, Erwin
[2
]
机构:
[1] Korea Univ, Dept Adv Mat Chem, Jochiwon 339700, South Korea
[2] Queens Univ, Dept Chem, Kingston, ON K7L 3N6, Canada
关键词:
NMR;
1H NMR;
13C NMR;
1D NMR;
2D NMR;
(2Z,2'E)-2,2'-(2-phenyl propane-1,3-diylidene) bis(1,3,3-trimethylindoline);
(2Z,2'E)-2,2'-(2-phenyl propane-1,3-diylidene) bis(5-chloro-1,3,3-trimethylindoline);
three-bladed propeller conformations;
D O I:
10.1002/mrc.2255
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
The H-1 and C-13 NMR spectra of the novel heterocyclic Leuco-TAM dyes, (2Z,2'E)-2,2'-(2-phenyl propane-1,3-diylidene) bis(1,3,3-trimethylindoline) derivatives 1-4 as precursors of triarylmethane (TAM)+ (Malachite Green FB-analog) dyes were completely assigned by 1D and 2D NMR experiments, including DEPT, COSY, HSQC, HMBC, and NOESY. Especially, the diastereotopic gem-dimethyl protons at the C3 and C3' positions of the FB rings were definitively assigned. The (Z,E) isomers adopt the energetically favored three-bladed propeller conformation in solution. Copyright (c) 2008 John Wiley & Sons, Ltd.
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页码:872 / 877
页数:6
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