Synthesis and X-ray crystallographic characterization of substituted aryl imines
We report the synthesis of α-diimine 1,4-bis(2,5-di- tert-butylphenyl)-2,3-dimethyl-1,4-diaza-1,3-butadiene, 1, and α-iminoketones 2-[(3,5-xylyl)imino]acenaphthylen-1-one, 4, and 2-[(4-chlorophenyl)imino]acenaphthylen-1-one, 5, all of which have been characterized by 1H NMR, 13C NMR, IR, and X-ray c...
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Veröffentlicht in: | Journal of molecular structure 2011-04, Vol.992 (1), p.33-38 |
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Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | We report the synthesis of α-diimine 1,4-bis(2,5-di-
tert-butylphenyl)-2,3-dimethyl-1,4-diaza-1,3-butadiene,
1, and α-iminoketones 2-[(3,5-xylyl)imino]acenaphthylen-1-one,
4, and 2-[(4-chlorophenyl)imino]acenaphthylen-1-one,
5, all of which have been characterized by
1H NMR,
13C NMR, IR, and X-ray crystallography. Also, we report the previously unknown X-ray crystal structures of α-diimines Ar-BIAN (Ar-BIAN
=
bis(arylimino)acenaphthene; Ar
=
3,5-xylyl,
2; Ar
=
4-chlorophenyl,
3) and α-iminoketone 2-[(2,6-xylyl)imino]acenaphthylen-1-one,
6. In solution,
4 and
5 show fluxional behavior observed with variable temperature
1H NMR in DMSO-
d
6 which is attributed to isomerization between the
E and
Z form of the imine. |
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ISSN: | 0022-2860 1872-8014 |
DOI: | 10.1016/j.molstruc.2011.02.027 |