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Published in 2023 at "Advanced Functional Materials"
DOI: 10.1002/adfm.202211853
Abstract: Deep‐red (DR)‐to‐near‐infrared (NIR) phosphorescent organic light‐emitting diodes (OLEDs) have potentials for application in various fields ranging from phototherapy to sensing. Accordingly, herein, phenylpyridazine‐based bidentate ligands are synthesized and subsequently utilized for the preparation of dinuclear…
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Keywords:
engineering shortening;
deep red;
molecular engineering;
red near ... See more keywords
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1
Published in 2020 at "ChemPlusChem"
DOI: 10.1002/cplu.202000384
Abstract: We report the synthesis, characterization, and photophysical and ion-binding properties of deep-red to near-infrared (NIR) fluorescent rhodamine derivatives, bearing two spirolactone rings and substitution of the oxygen atoms in the xanthene ring with sulfur atoms…
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Keywords:
red near;
infrared nir;
nir fluorescent;
near infrared ... See more keywords
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Published in 2018 at "Macromolecular rapid communications"
DOI: 10.1002/marc.201800034
Abstract: Photocleavable polymers have attracted much attention in drug delivery, photopatterning, and controlling cell behavior. Photolysis is usually induced by UV light. However, UV light cannot penetrate deeply into biological tissue and may damage biological components.…
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Keywords:
red near;
cleavable polymers;
light cleavable;
near infrared ... See more keywords
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Published in 2021 at "Dyes and Pigments"
DOI: 10.1016/j.dyepig.2021.109289
Abstract: Abstract In this work, we synthesized a novel long-wavelength-emitting fluorophore FQ-OH based on a novel designed hydroxylflavone-quinoline-amino molecular system with both intramolecular charge transfer (ICT) and excited-state intramolecular proton transfer (ESIPT) process, enabling FQ-OH with…
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Keywords:
near infrared;
red near;
based novel;
hydroxylflavone quinoline ... See more keywords
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Published in 2017 at "Materials Letters"
DOI: 10.1016/j.matlet.2017.04.060
Abstract: Abstract Near-infrared to visible and near-infrared upconversion emission has been reported in Yb 3+ /Ln 3+ (Ln 3+ = Er 3+ /Tm 3+ /Ho 3+ )-α-sialon ceramic prepared by hot press sintering technique. Under 980 nm excitation,…
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Keywords:
red near;
infrared emissions;
near infrared;
green red ... See more keywords
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Published in 2018 at "Nature Communications"
DOI: 10.1038/s41467-018-05040-8
Abstract: Considerable achievements on multiple emission capabilities and tunable wavelengths have been obtained in inorganic luminescent materials. However, the development of organic counterparts remains a grand challenge. Herein we report a series of 2-/2,6-aryl substituted boron-dipyrromethene…
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Keywords:
red near;
emissions across;
aryl substituted;
across red ... See more keywords
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Published in 2017 at "Chemical communications"
DOI: 10.1039/c6cc09186e
Abstract: Two slightly twisted A-π-D-π-A molecules were prepared to demonstrate that the red/near-infrared mechanoresponsive luminescence turn-on behaviors could be realized through mechanically disturbing their weakly/non-emissive metastable nanostructures, giving emissive amorphous aggregates with λem = 620 nm,…
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Keywords:
red near;
metastable nanostructures;
near infrared;
mechanoresponsive luminescence ... See more keywords
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1
Published in 2018 at "Nanoscale"
DOI: 10.1039/c8nr01981a
Abstract: Semiconductor quantum dots (QDs) are promising luminescent materials for use in lighting, display and bio-imaging, and the color tuning is a necessity for such applications. In this work, we report tunable colors and deep-red or…
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Keywords:
red near;
near infrared;
zns;
deep red ... See more keywords
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Published in 2019 at "Journal of Materials Chemistry C"
DOI: 10.1039/c9tc03645h
Abstract: Highly efficient deep-red/near-infrared emissions with maximum EQEs of 7.04% and 4.14%, respectively, are realized for Ir(iii) complexes by designing rigid fused-heterocyclic ligands.
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Keywords:
efficient deep;
near infrared;
red near;
deep red ... See more keywords
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Published in 2022 at "Chemical Science"
DOI: 10.1039/d2sc04601f
Abstract: Molecular photoswitches operating in the red to near-IR region with controllable thermal relaxation rates are attractive components for photo-regulating biological processes. Herein, we report the synthesis of red-shifted azobenzenes functionalised with the heavier chalcogens and…
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Keywords:
periodic trends;
chalcogen halogen;
red near;
chalcogen bonding ... See more keywords