2007
DOI: 10.1016/j.saa.2006.12.015
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X-ray diffraction and IR spectral characteristics of zinc(II)tetra-tert-butylphthalocyanine

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Cited by 14 publications
(14 citation statements)
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“…The spectra of the isomers of H 2 (3 tert Bu)Pc and H 2 (4 tert Bu)Pc are very sim ilar [34]. This fact was confirmed experimentally for Zn(tert Bu) 4 Pc [21]. The introduction of four tert butyl groups in the MPc molecule results in some spectral changes; in particular, the intensity and position of some bands change and some new bands arise, but in general the shape of the spectrum remains the same ( Table 5).…”
Section: Polymorphic Forms Of Mpcs and Their Characteristicsmentioning
confidence: 71%
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“…The spectra of the isomers of H 2 (3 tert Bu)Pc and H 2 (4 tert Bu)Pc are very sim ilar [34]. This fact was confirmed experimentally for Zn(tert Bu) 4 Pc [21]. The introduction of four tert butyl groups in the MPc molecule results in some spectral changes; in particular, the intensity and position of some bands change and some new bands arise, but in general the shape of the spectrum remains the same ( Table 5).…”
Section: Polymorphic Forms Of Mpcs and Their Characteristicsmentioning
confidence: 71%
“…The majority of X ray data are obtained for unsubstituted metal phthalocyanines. The exception is works [19][20][21], which are devoted to the study of alkyl and alkoxy substituted MPcs. The introduction of four tert butyl groups contributes to a looser crystal packing (Table 2).…”
Section: Polymorphic Forms Of Mpcs and Their Characteristicsmentioning
confidence: 99%
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“…On the other hand, Figures 2c and 3c do not show clear peak at around 600 nm. The peak at around 600 nm as shown in Figures 2a, 2b, 3a, and 3b is ascribed to the a-type crystalline form of H 2 TTBPc [10][11]. In particular, it is clear that the electrospinning of H 2 TTBPc=C 60 =PVP increased the absorption peak at around 600 nm as shown in Figure 2a.…”
Section: Spectroscopic Characterizationmentioning
confidence: 81%