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Sökning: id:"swepub:oai:DiVA.org:kth-195127" > An AIE and ICT base...

An AIE and ICT based NIR florescent probe for cysteine and homocysteine

Bu, L. (författare)
Chen, J. (författare)
Wei, X. (författare)
visa fler...
Li, Xin (författare)
KTH,Teoretisk kemi och biologi
Ågren, Hans (författare)
KTH,Teoretisk kemi och biologi
Xie, Y. (författare)
visa färre...
 (creator_code:org_t)
Elsevier BV, 2017
2017
Engelska.
Ingår i: Dyes and pigments. - : Elsevier BV. - 0143-7208 .- 1873-3743. ; 136, s. 724-731
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • A combination of aggregation-induced emission and intramolecular charge transfer was achieved by using a triphenylamine analogue and a dicyanovinyl moiety as the electron donating and accepting units, respectively. Hence, we designed and synthesized a probe with a D-π-A framework as a near-infrared fluorescence turn-on probe for biothiols (cysteine and homocysteine). Owing to the remarkable intramolecular charge transfer effect as well as intramolecular rotations associated with the donor moiety, the probe exhibits extremely weak fluorescence, which becomes a good starting point for developing fluorescence “turn-on” probes. Upon reaction with cysteine or homocysteine utilizing the dicyanovinyl moiety, the intramolecular charge transfer character was weakened, and the reacting products were observed to aggregate in aqueous solutions, resulting in the aggregation-induced emission effect with red fluorescence at 651 and 656 nm, respectively. Hence, the probe could be used as a fluorescence “turn-on” sensor for cysteine and homocysteine, with the sensing time of less than 4 min and the detection limits of 8.4 μM and 5.7 μM towards cysteine and homocysteine, respectively. The probe could distinguish cysteine and homocysteine from glutathione. The sensing mechanism was systematically investigated by employing high resolution mass spectrometry, 1H NMR and density functional theory calculations as well as checking the solvent viscosity dependent fluorescence, and thus the nucleophilic addition products, the intramolecular charge transfer character, and the aggregation-induced emission behaviour were clearly elucidated. It is noteworthy that the low cytotoxicity, the intrinsic aggregation-induced emission nature and near-infrared emissions enable the application of the probe in living cell imaging.

Ämnesord

NATURVETENSKAP  -- Kemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences (hsv//eng)

Nyckelord

AIE
Biothiols
Cell imaging
Fluorescent probes
ICT
Addition reactions
Amino acids
Charge transfer
Density functional theory
Fluorescence
Infrared devices
Lanthanum compounds
Mass spectrometry
Solutions
Aggregation-induced emissions
High resolution mass spectrometry
Intra-molecular charge transfer
Near-infrared emissions
Near-infrared fluorescence
Probes

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ref (ämneskategori)
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Av författaren/redakt...
Bu, L.
Chen, J.
Wei, X.
Li, Xin
Ågren, Hans
Xie, Y.
Om ämnet
NATURVETENSKAP
NATURVETENSKAP
och Kemi
Artiklar i publikationen
Dyes and pigment ...
Av lärosätet
Kungliga Tekniska Högskolan

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