2012
DOI: 10.5155/eurjchem.3.2.163-171.538
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Solvent effect on the spectral properties of dipolar laser dyes: Evaluation of ground and excited state dipole moments

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Cited by 14 publications
(3 citation statements)
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References 47 publications
(53 reference statements)
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“…Furthermore, the bathochromic shift observed in both absorption and fluorescence spectra (see Table 1 and the Supporting Information) with increasing solvent polarity (compare spectra for solvents that do not donate hydrogen bonds, such as MeCN and DMSO, or compare spectra for different protic solvents, such as MeOH and aqueous buffer) suggests that the fluorescence involves the π→π* transition. Such a solvent effect on the spectral properties of sulforhodamines has been recently reported for the commercial sulforhodamine B and meaningfully interpreted through the evaluation of ground‐ and excited‐state dipole moments of this dye 24. As revealed by fluorescence emission profiles shown in Figure 1 (and those available in the Supporting Information), all these unsymmetrical sulforhodamines exhibit an intense emission peak with a maximum in the range 567–638 nm.…”
Section: Methodssupporting
confidence: 67%
“…Furthermore, the bathochromic shift observed in both absorption and fluorescence spectra (see Table 1 and the Supporting Information) with increasing solvent polarity (compare spectra for solvents that do not donate hydrogen bonds, such as MeCN and DMSO, or compare spectra for different protic solvents, such as MeOH and aqueous buffer) suggests that the fluorescence involves the π→π* transition. Such a solvent effect on the spectral properties of sulforhodamines has been recently reported for the commercial sulforhodamine B and meaningfully interpreted through the evaluation of ground‐ and excited‐state dipole moments of this dye 24. As revealed by fluorescence emission profiles shown in Figure 1 (and those available in the Supporting Information), all these unsymmetrical sulforhodamines exhibit an intense emission peak with a maximum in the range 567–638 nm.…”
Section: Methodssupporting
confidence: 67%
“…The variable α represents the solvent hydrogen-bond donor (HBD) acidity and is considered as the solvent's ability to donate a proton in a solvent-to-solute hydrogen bond. The variable β represents solvent hydrogen-bond acceptor (HBA) basicity and is considered as the solvent's ability to accept a proton in a solute-to-solvent hydrogen bond [48,49]. The correlation coefficients, MCCs, are greater than 0.5 in absorption and emission spectra (except for compound IV in absorption spectra), revealing the applicability of Kamlet- Taft Tables 13 and 14.…”
Section: Kamlet and Taft Methodsmentioning
confidence: 99%
“…To provide the inks with luminescent properties, two different dyes were employed: (i) fluorescein 27 (F27), a luminescent dye having an emission centered at 520 nm (green light) [48,49]; and (ii) Rhodamine B, which strongly absorbs in the green and emits light in the orange-red region of the spectrum, centered at 585 nm [50]. F27 and Rhodamine B were purchased from Lambda Physic under the references Lambdachrome LC 5530 and LC6100, respectively.…”
Section: Methodsmentioning
confidence: 99%