Arylether substituted diacetylenes with spacing groups of different length. A comparative study of their distinct solid state reactivities
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Research context
OpenAlex topics: Polydiacetylene-based materials and applications · Synthesis and Properties of Aromatic Compounds · Porphyrin and Phthalocyanine Chemistry
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References (12)
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1. 1985
2. Enkelmann · 1984 · 91
3. Dauber · Acc. Chem. Res. · 1980 · 13 · 10510.1021/ar50148a002 ↗
4. Gavezzotti · Chem. Rev. · 1982 · 82 · 110.1021/cr00047a001 ↗
5. Veciana · Mol. Cryst. Liq. Cryst. · 1988 · 156 · 28910.1080/00268948808070578 ↗
6. J. Veciana et al., manuscript in preparation.
7. Kalyanaraman · Makromol. Chem. · 1979 · 180 · 139310.1002/macp.1979.021800531 ↗
8. Wegner · Z. Naturforsch · 1969 · 24b · 82410.1515/znb-1969-0708 ↗
9. Satisfactory elemental analyses and spectral data (I.R., 1H NMR, 13C NMR, UV-vis and mass spectrometry) have been obtained for all new compounds 2a-d, 3a-d, 4 (n=2,3), 5 (n=2,3), and 6a-c (n=2, 3).
10. sanger · Biochem. J. · 1945 · 39 · 50710.1042/bj0390507 ↗
11. Armitage · J. Chem. Soc. · 1959 · 1998
12. From a detailed revision of crystal structures of DA's using the Cambridge Structural Data Base. J. Veciana et al., to be published.