Articles with "nir probes" as a keyword



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Fluorogenic NIR-probes based on 1,2,4,5-tetrazine substituted BF2-azadipyrromethenes.

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Published in 2017 at "Chemical communications"

DOI: 10.1039/c7cc06545k

Abstract: A series of 1,2,4,5-tetrazine integrated near infrared (NIR) fluorophores based on the BF2 azadipyrromethene (NIR-AZA) class has been synthesised and their ability to modulate emission from low to high in response to Diels-Alder cycloaditions has… read more here.

Keywords: fluorogenic nir; probes based; based tetrazine; nir ... See more keywords
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Asymmetric Si-rhodamine scaffolds: rational design of pH-durable protease-activated NIR probes in vivo.

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Published in 2020 at "Chemical communications"

DOI: 10.1039/c9cc09666c

Abstract: A group of asymmetric Si-rhodamine scaffolds was designed for protease-activated NIR probes. Dual pH-inertia for both spirocyclized fluorescent probes and fluorescent products of zwitterions form over a wide range of pH (4.0-11.0). Leucine aminopeptidase (LAP)… read more here.

Keywords: asymmetric rhodamine; protease activated; activated nir; nir probes ... See more keywords
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Activatable BODIPY-Chromene NIR-II probes with small spectral crosstalk endow high-contrast in vivo bioimaging

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Published in 2023 at "Chemical Communications"

DOI: 10.1039/d3cc01742g

Abstract: Herein, we design a novel "crossbreeding" dye (BC-OH) within the second near-infrared (NIR-II) window based on BODIPY and Chromene chromophores. BC-OH can serve as a platform to construct activatable NIR-II... read more here.

Keywords: activatable bodipy; bodipy chromene; chromene; chromene nir ... See more keywords