Abstract Changes in the viscosity of intracellular microenvironments may indicate the onset of diseases like diabetes, blood‐based illnesses, hypertension, and Alzheimer's. To date, monitoring viscosity changes in the intracellular environment remains a challenge with prior work focusing primarily on visible light‐absorbing viscosity sensing fluorophores. Herein, a series of near‐infrared (NIR, 700–1000 nm) absorbing and emitting indolizine squaraine fluorophores (1PhSQ,2PhSQ,SO3SQ,1DMASQ,7DMASQ, and1,7DMASQ) are synthesized and studied for NIR viscosity sensitivity.2PhSQexhibits a very high slope in its Forster‐Hoffmann plot at 0.75 which indicates this dye is a potent viscosity sensor. The properties of the squaraine fluorophores are studied computationallyviadensity functional theory (DFT) and time‐dependent (TD)‐DFT. Experimentally, both steady‐state and time‐resolved emission spectroscopy, absorption spectroscopy, and electrochemical characterization are conducted on the dyes. Precise photophysical tuning is observed within the series with emission maxima wavelengths as long as 881 nm for1,7DMASQand fluorescence quantum yields as high as 39.5 and 72.0 % for1PhSQin DCM and THF, respectively. The high tunability of this molecular scaffold renders indolizine squaraine fluorophores excellent prospects as viscosity‐sensitive biological imaging agents with2PhSQgiving a dramatically higher fluorescence quantum yield (from 0.3 to 37.1 %) as viscosity increases. 
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                            Bright NIR‐II Photoluminescence in Rod‐Shaped Icosahedral Gold Nanoclusters
                        
                    
    
            Abstract Fluorophores with high quantum yields, extended maximum emission wavelengths, and long photoluminescence (PL) lifetimes are still lacking for sensing and imaging applications in the second near‐infrared window (NIR‐II). In this work, a series of rod‐shaped icosahedral nanoclusters with bright NIR‐II PL, quantum yields up to≈8%, and a peak emission wavelength of 1520 nm are reported. It is found that the bright NIR‐II emission arises from a previously ignored state with near‐zero oscillator strength in the ground‐state geometry and the central Au atom in the nanoclusters suppresses the non‐radiative transitions and enhances the overall PL efficiency. In addition, a framework is developed to analyze and relate the underlying transitions for the absorptions and the NIR‐II emissions in the Au nanoclusters based on the experimentally defined absorption coefficient. Overall, this work not only shows good performance of the rod‐shaped icosahedral series of Au nanoclusters as NIR‐II fluorophores, but also unravels the fundamental electronic transitions and atomic‐level structure‐property relations for the enhancement of the NIR‐II PL in gold nanoclusters. The framework developed here also provides a simple method to analyze the underlying electronic transitions in metal nanoclusters. 
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                            - PAR ID:
- 10452770
- Publisher / Repository:
- Wiley Blackwell (John Wiley & Sons)
- Date Published:
- Journal Name:
- Small
- Volume:
- 17
- Issue:
- 11
- ISSN:
- 1613-6810
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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