Articles with "helicene" as a keyword



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DNA-induced circularly polarized luminescence of helicene racemates.

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Published in 2023 at "Chirality"

DOI: 10.1002/chir.23566

Abstract: Enantiopure helicenes have been extensively investigated due to their outstanding chiroptical properties, while helicene racemates are considered as chiroptically silent. Here, we describe a facile method to produce circularly polarized luminescence (CPL) from helicene racemates… read more here.

Keywords: dna; helicene; helicene racemates; polarized luminescence ... See more keywords
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Detection of hazardous mercury ion using [5]helicene-based fluorescence probe with "TurnON" sensing response for practical applications.

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Published in 2021 at "Journal of hazardous materials"

DOI: 10.1016/j.jhazmat.2021.126242

Abstract: A new fluorescence probe based on [5]helicene derivative (MT) was designed and synthesized. The chemical structure of the probe was fully characterized by NMR, mass spectrometry and X-ray crystallography. MT which is the combination of… read more here.

Keywords: hg2; response; fluorescence; probe ... See more keywords
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Synthesis and properties of a thiophene-substituted diaza[7]helicene for application as a blue emitter in organic light-emitting diodes

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Published in 2017 at "Tetrahedron Letters"

DOI: 10.1016/j.tetlet.2016.12.069

Abstract: Abstract Carbazole-based diaza[7]helicene substituted by thiophene groups, 2,12-dithiophene-5,15-dihexyl-5,15-diaza[7]helicene ( 6 ), was synthesised successfully and confirmed by 1 H NMR, 13 C NMR, High Resolution Mass Spectrometry, Time of Flight Mass Spectrometry. Compound 6 exhibited… read more here.

Keywords: helicene; synthesis properties; thiophene substituted; properties thiophene ... See more keywords
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Synthesis, Crystal Analysis, and Physical Properties of Double [6]helicene-Containing Heteroarenes with Circularly Polarized Luminescence.

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Published in 2022 at "Organic letters"

DOI: 10.1021/acs.orglett.2c03786

Abstract: Two novel helical heteronanographenes bearing a [6]helicene unit (3a and 5a) have been synthesized, and their molecular structures are unambiguously determined via single-crystal X-ray diffraction analyses. Density functional theory calculations suggest that the as-prepared compounds… read more here.

Keywords: synthesis crystal; properties double; physical properties; helicene ... See more keywords
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Intramolecular Azo Coupling Reaction of Binaphthyl Compounds: Synthesis of Pyrazole-Containing Helicene-Like Molecules.

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Published in 2023 at "Organic letters"

DOI: 10.1021/acs.orglett.3c00974

Abstract: A method for accessing pyrazole-containing helicene-like molecules from easily accessible NOBIN derivatives was developed. The reaction proceeded efficiently via diazonium salt intermediates, which provided a series of helicene-like molecular products in yields of 77%-89% regardless… read more here.

Keywords: containing helicene; reaction; helicene like; helicene ... See more keywords
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Modification of [5]Helicene with Dimesitylboryl: One Way To Enhance the Fluorescence Efficiency.

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Published in 2018 at "Organic letters"

DOI: 10.1021/acs.orglett.8b03329

Abstract: The efficient synthetic route was disclosed to prepare structurally asymmetric [5]helicenes, which are substituted with either BMes2 (7B-HC) or both BMes2 and NMe2 (8B5NMe2-HC, 7B5NMe2-HC). Compared with the parent [5]helicene, these compounds show greatly enhanced… read more here.

Keywords: helicene dimesitylboryl; helicene; fluorescence; dimesitylboryl one ... See more keywords
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Stable Double and Quadruple [5]Helicene Derivatives: Synthesis, Structural Analysis, and Physical Properties.

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Published in 2019 at "Organic letters"

DOI: 10.1021/acs.orglett.9b04246

Abstract: Two novel [5]helicene derivatives (labeled 5 and 8) have been successfully synthesized and characterized. The structural analyses, photophysical properties, along with density functional theory calculations for unveiling the helicity inversion and equilibrium of the diastereomers,… read more here.

Keywords: helicene; double quadruple; quadruple helicene; derivatives synthesis ... See more keywords
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Single-Handed Helicene Nanoribbons via Transfer of Chiral Information.

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Published in 2022 at "Journal of the American Chemical Society"

DOI: 10.1021/jacs.2c09288

Abstract: Here we show the access to single-handed helicene nanoribbons by utilizing a [6]helicene building block to induce diastereoselective, photochemical formation of [5]helicene units. Specifically, we have synthesized nanoribbons P1 and P2 with different ratios of… read more here.

Keywords: information; nanoribbons via; helicene nanoribbons; helicene ... See more keywords
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Synthesis, structure and photophysical properties of a 2D network with gold dicyanide donors coordinated to aza[5]helicene viologen acceptors.

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Published in 2019 at "Dalton transactions"

DOI: 10.1039/c9dt01823a

Abstract: A recently synthesized photoluminescent organic acceptor, 5,10-dimethyl-5,10-diaza[5]helicene is shown to react with dicyanoaurate anions to form a 2D network N,N-dimethylaza[5]helicene dicyanoaurate. The structure of the synthesized complex was investigated via X-ray crystallography showing the presence… read more here.

Keywords: helicene; network; dimethyl diaza; transfer ... See more keywords
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Synthesis of a helicene-fused porphyrin leading to a π-extended chiral chromophore.

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Published in 2022 at "Chemical communications"

DOI: 10.1039/d2cc01475k

Abstract: The preparation of several covalently linked [6]-helicene-porphyrins is reported. A fused [6]-helicene-porphyrin π-extended aromatic system was isolated, the enantiomers separated and the chiroptical properties determined. The oxidative cyclodehydrogenation proved to be very effective for six-membered… read more here.

Keywords: helicene fused; porphyrin leading; leading extended; helicene ... See more keywords
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Helicene-based π-conjugated macrocycles: their synthesis, properties, chirality and self-assembly into molecular stripes on a graphite surface.

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Published in 2022 at "Nanoscale"

DOI: 10.1039/d2nr04209f

Abstract: Fully aromatic helicenes are attractive building blocks for the construction of inherently chiral π-conjugated macrocyclic nanocarbons. These hitherto rare molecular architectures are envisaged to exhibit remarkable (chir)optical properties, self-assembly, charge/spin transport, induced ring current or… read more here.

Keywords: cyclic trimer; molecular stripes; helicene cyclic; self assembly ... See more keywords