Articles with "red near" as a keyword



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Molecular Engineering for Shortening the Pt···Pt Distances in Pt(II) Dinuclear Complexes and Enhancing the Efficiencies of these Complexes for Application in Deep‐Red and Near‐IR OLEDs

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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… read more here.

Keywords: engineering shortening; deep red; molecular engineering; red near ... See more keywords
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A Deep-Red to Near Infrared (NIR) Fluorescent Probe Based on a Sulfur-Modified Rhodamine Derivative with Two Spirolactone Rings.

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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… read more here.

Keywords: red near; infrared nir; nir fluorescent; near infrared ... See more keywords
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Red and Near-Infrared Light-Cleavable Polymers.

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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.… read more here.

Keywords: red near; cleavable polymers; light cleavable; near infrared ... See more keywords
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A red-to-near-infrared fluorescent probe for the detection of thiophenol based on a novel hydroxylflavone-quinoline-amino molecular system with large Stokes shift

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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… read more here.

Keywords: near infrared; red near; based novel; hydroxylflavone quinoline ... See more keywords
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Blue, green, red and near-infrared emissions via upconversion in α-sialon

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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,… read more here.

Keywords: red near; infrared emissions; near infrared; green red ... See more keywords
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Domino-like multi-emissions across red and near infrared from solid-state 2-/2,6-aryl substituted BODIPY dyes

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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… read more here.

Keywords: red near; emissions across; aryl substituted; across red ... See more keywords
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Achieving red/near-infrared mechanoresponsive luminescence turn-on: mechanically disturbed metastable nanostructures in organic solids.

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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,… read more here.

Keywords: red near; metastable nanostructures; near infrared; mechanoresponsive luminescence ... See more keywords
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Achieving deep-red-to-near-infrared emissions in Sn-doped Cu-In-S/ZnS quantum dots for red-enhanced white LEDs and near-infrared LEDs.

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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… read more here.

Keywords: red near; near infrared; zns; deep red ... See more keywords
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Iridium(iii) phosphors with rigid fused-heterocyclic chelating architectures for efficient deep-red/near-infrared emissions in polymer light-emitting diodes

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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. read more here.

Keywords: efficient deep; near infrared; red near; deep red ... See more keywords
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Fast relaxing red and near-IR switchable azobenzenes with chalcogen and halogen substituents: periodic trends, tuneable thermal half-lives and chalcogen bonding

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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… read more here.

Keywords: periodic trends; chalcogen halogen; red near; chalcogen bonding ... See more keywords