1996
DOI: 10.1016/s0032-3861(96)00414-4
|View full text |Cite
|
Sign up to set email alerts
|

Quenching in the excited singlet state of amphiphilic copolymers with pendant carbazolylalkyl groups in aqueous solution

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1

Citation Types

3
17
0

Year Published

2001
2001
2018
2018

Publication Types

Select...
5

Relationship

1
4

Authors

Journals

citations
Cited by 10 publications
(20 citation statements)
references
References 17 publications
3
17
0
Order By: Relevance
“…Relative fluorescence quantum yields (Φ r ) were determined by comparing the area for the corrected spectra. The copolymerizations of AMPS and the present (meth)acrylamides gave highly random copolymers, as in the previous cases [1,4]. The results of polymerization for poly(CzEMAm-co-AMPS) [r-CzEMAm(x)], as a typical example, are shown in Table 1.…”
Section: Measurementssupporting
confidence: 61%
See 3 more Smart Citations
“…Relative fluorescence quantum yields (Φ r ) were determined by comparing the area for the corrected spectra. The copolymerizations of AMPS and the present (meth)acrylamides gave highly random copolymers, as in the previous cases [1,4]. The results of polymerization for poly(CzEMAm-co-AMPS) [r-CzEMAm(x)], as a typical example, are shown in Table 1.…”
Section: Measurementssupporting
confidence: 61%
“…Figure 2 shows the fluorescence spectra of poly(CzMMAm-co-AMPS) [r-CzMMAm(x)] in DMF. As in the case of poly(CzPMAm-co-AMPS) [r-CzPMAm(x)] [1], all the copolymers showed a structured monomer emission which decayed exponentially [the lifetime (t) = 12.8 AE 0.5 nsec], indicating that this type of copolymers are free of excimer formation and self-quenching in DMF. The spectra of r-CzMMAm(x) and poly(CzMAAm-co-AMPS) [r-CzMAAm(x)], are essentially the same, were slightly broadened and blue-shifted by ca.…”
Section: Measurementsmentioning
confidence: 74%
See 2 more Smart Citations
“…At this point, we attribute the reduction of the quantum yield for copolymers with higher dye content to concentration quenching. This phenomenon was shown, for instance, by Itoh et al for copolymers containing dyes with known aggregation caused quenching behavior [53] where lower ratios of the incorporated dye minimize the quenching originating from intra-and intermolecular aggregation. For the cyanine-containing copolymers 6a-d, a maximum quantum yield of 13% for 6a was achieved ( Figures S37-S40, Supporting Information).…”
Section: Fluorescence Propertiesmentioning
confidence: 74%