2012
DOI: 10.1016/j.saa.2012.05.047
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Experimental (FT-IR, FT-Raman and UV–Vis) spectra and theoretical DFT investigations of 2,3-diaminophenazine

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Cited by 19 publications
(10 citation statements)
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“…Before characterizations, the nal product that was separated from reaction solution by centrifugation was carried out through cooling crystallization, centrifugation and desiccation to form a needle-like crystal (Scheme 1C). 34 Based on above characterizations, we can identify that the obtained product is DAP. 3(a) shows the IR spectrum of the crystal.…”
Section: Identication Of the Opd-oxidized Productmentioning
confidence: 99%
See 1 more Smart Citation
“…Before characterizations, the nal product that was separated from reaction solution by centrifugation was carried out through cooling crystallization, centrifugation and desiccation to form a needle-like crystal (Scheme 1C). 34 Based on above characterizations, we can identify that the obtained product is DAP. 3(a) shows the IR spectrum of the crystal.…”
Section: Identication Of the Opd-oxidized Productmentioning
confidence: 99%
“…3(a), it proves that the product of the OPD-oxidized reaction is DAP, which is similar to the previously reported DAP molecules. 33,34 Fig. 3(b) displays the MS of the product.…”
Section: Identication Of the Opd-oxidized Productmentioning
confidence: 99%
“…The embedded micro-photographic image in Figure 3 shows the dried spot of concentrated sample, spiked with six cells of Salmonella. The characteristic peaks of Safranin O marked at 615, 759, 1202, 1377, 1556, and 1641cm −1 noticeably appear in each trace of Figure 3 [ 30 , 31 ]. The assignments of these peaks to each corresponding vibration modes are listed in the Appendix B section.…”
Section: Resultsmentioning
confidence: 99%
“…17 Through density functional theory (DFT) calculations Sylvestre et al have performed vibration analysis and natural bond orbital analysis of DAP. 18 Vibrational analysis indicates simultaneous existence of the C-C stretching mode for both its IR and Raman spectra thereby allowing delocalization of charge from electron donating amino groups to the phenazine ring. Additionally, the theoretically computed HOMO and LUMO energy gap closely matches with the observed  max peak at 419 nm in its UV-visible absorption spectrum (Figure 2A).…”
mentioning
confidence: 99%
“…Molecular electrostatic potential (MEP) analysis also revealed the highest degree of negative charge accumulation to be on the pyrazine nitrogen atoms ( Figure 2B). 18 Expectedly the 2,3-diamino group in 4 being a stronger electron donor than the 2,3-dialkoxy groups in 8 and 10 (Scheme 1) as reflected in the para-Hammett constants ( p values for -NH 2 is -0.66 and for -OEt is -0.25), 19 the extent of ICT in 4 is higher than that in 8 and 10 which is why the corresponding  max is modestly red-shifted (419 nm over 410 nm). A pH sensitive imidazole-fused phenazine 11 was reported by Ryazanova et.…”
mentioning
confidence: 99%