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Huimin Guo

Researcher at Dalian University of Technology

Publications -  74
Citations -  6478

Huimin Guo is an academic researcher from Dalian University of Technology. The author has contributed to research in topics: Phosphorescence & Excited state. The author has an hindex of 41, co-authored 74 publications receiving 5870 citations. Previous affiliations of Huimin Guo include Chinese Academy of Sciences & Dalian Institute of Chemical Physics.

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Excited state intramolecular proton transfer (ESIPT): from principal photophysics to the development of new chromophores and applications in fluorescent molecular probes and luminescent materials.

TL;DR: The basic photophysics of the excited-state intramolecular proton transfer (ESIPT) chromophores are introduced and the state-of-the-art development of the ESIPT chromophore and their applications in chemosensors, biological imaging and white-light emitting materials are summarized.
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Triplet–triplet annihilation based upconversion: from triplet sensitizers and triplet acceptors to upconversion quantum yields

TL;DR: In this paper, the authors focus on the reported TTA based upconversion examples, the challenges that are facing the developments of TTA up-conversion and the design rationales for the triplet sensitizers and triplet acceptors.
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Organic Triplet Sensitizer Library Derived from a Single Chromophore (BODIPY) with Long-Lived Triplet Excited State for Triplet–Triplet Annihilation Based Upconversion

TL;DR: A library of organic triplet sensitizers based on a single chromophore of boron-dipyrromethene (BODIPY) is proposed, paving the way for the design and applications in photovoltaics and upconversions, etc.
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A highly selective red-emitting FRET fluorescent molecular probe derived from BODIPY for the detection of cysteine and homocysteine: an experimental and theoretical study

TL;DR: A red-emitting BODIPY-based fluorescent-resonance-energy-transfer (FRET) molecular probe 1 for selective detection of cysteine and homocysteine was designed and used for in vivo fluorescent imaging of cellular thiols.
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Geometry relaxation-induced large Stokes shift in red-emitting borondipyrromethenes (BODIPY) and applications in fluorescent thiol probes.

TL;DR: DFT calculations propose the large Stokes shifts of BS-SS and BS-DS are due to the remarkable geometry relaxation upon photoexcitation and its substantial effect on the energy levels of molecular orbitals.