4,5-Diazafluorene co-oligomers as electrondeficientlight-emitting materials and selectivefluorescence sensors for mercury(II) cations
Research output: Contribution to journal › Article › peer-review
Standard Standard
In: Journal of Materials Chemistry C, Vol. 6, No. 14, 14.04.2018, p. 3762-3773 .
Research output: Contribution to journal › Article › peer-review
HarvardHarvard
APA
CBE
MLA
VancouverVancouver
Author
RIS
TY - JOUR
T1 - 4,5-Diazafluorene co-oligomers as electrondeficientlight-emitting materials and selectivefluorescence sensors for mercury(II) cations
AU - Ghosh, Sanjay
AU - Alghunaim, Abulaziz S.
AU - AL-Mashhadani, Mohammed
AU - Krompiec, Michal Piotr
AU - Hallett, Megan
AU - Perepichka, Igor
PY - 2018/4/14
Y1 - 2018/4/14
N2 - A series of 4,5-diazafluorene-based (N) conjugated co-oligomers with 9,9-dialkylfluorene (F) or electron-deficient dibenzothiophene-S,S-dioxide (S) has been synthesized by Pd-catalyzed coupling reaction (FNF, FFNFF, FNoF, SNS, NSN). Cyclic voltammetry studies reveal their improved electron affinity compared to oligofluorene. SNS and NSN co-oligomers showed a decrease of their LUMO energies by 0.37–0.38 eV compared to FNF co-oligomer. Absorption/emission studies showed that all oligomers, except FNoF, are blue-emitting materials (λPL ∼ 400–450 nm) with high quantum yields of their photoluminescence (ΦPL = 84–100% in solution and 24–42% in the solid state). FNoF trimer emits in the yellow region with a very low ΦPL ∼ 1% in dichloromethane solution, but the emission efficiency is substantially increased to ΦPL = 10–17% in the solid state. FNF co-oligomer was studied as a metal cation responsive colorimetric and fluorescent sensor using a series of mono- and divalent cations and it showed high sensitivity and selectivity toward mercury cations. Upon addition of Hg2+, the blue emission of FNF (λPL = 404 nm) was quenched and a new, bathochromically shifted (to the green region, λPL = 507 nm) emission band appeared, which allows this compound to be used as both an “ON → OFF” and “OFF → ON” fluorescent sensor.
AB - A series of 4,5-diazafluorene-based (N) conjugated co-oligomers with 9,9-dialkylfluorene (F) or electron-deficient dibenzothiophene-S,S-dioxide (S) has been synthesized by Pd-catalyzed coupling reaction (FNF, FFNFF, FNoF, SNS, NSN). Cyclic voltammetry studies reveal their improved electron affinity compared to oligofluorene. SNS and NSN co-oligomers showed a decrease of their LUMO energies by 0.37–0.38 eV compared to FNF co-oligomer. Absorption/emission studies showed that all oligomers, except FNoF, are blue-emitting materials (λPL ∼ 400–450 nm) with high quantum yields of their photoluminescence (ΦPL = 84–100% in solution and 24–42% in the solid state). FNoF trimer emits in the yellow region with a very low ΦPL ∼ 1% in dichloromethane solution, but the emission efficiency is substantially increased to ΦPL = 10–17% in the solid state. FNF co-oligomer was studied as a metal cation responsive colorimetric and fluorescent sensor using a series of mono- and divalent cations and it showed high sensitivity and selectivity toward mercury cations. Upon addition of Hg2+, the blue emission of FNF (λPL = 404 nm) was quenched and a new, bathochromically shifted (to the green region, λPL = 507 nm) emission band appeared, which allows this compound to be used as both an “ON → OFF” and “OFF → ON” fluorescent sensor.
U2 - 10.1039/C7TC05051H
DO - 10.1039/C7TC05051H
M3 - Article
VL - 6
SP - 3762
EP - 3773
JO - Journal of Materials Chemistry C
JF - Journal of Materials Chemistry C
SN - 2050-7526
IS - 14
ER -