BODIPY dyads and triads: synthesis, optical, electrochemical and transistor properties
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1752-153X
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
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online resource.
- Bibliographic citation
-
BODIPY dyads and triads: synthesis, optical, electrochemical and transistor properties ; volume:12 ; number:1 ; day:11 ; month:5 ; year:2018 ; pages:1-9 ; date:12.2018
Chemistry central journal ; 12, Heft 1 (11.5.2018), 1-9, 12.2018
- Creator
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Wanwong, Sompit
- Contributor
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Khomein, Piyachai
Thayumanavan, S.
SpringerLink (Online service)
- DOI
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10.1186/s13065-018-0430-5
- URN
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urn:nbn:de:101:1-2018071519022130520421
- Rights
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Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
15.08.2025, 7:33 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Wanwong, Sompit
- Khomein, Piyachai
- Thayumanavan, S.
- SpringerLink (Online service)
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Solvent and alkyl substitution effects on charge-transfer mediated triplet state generation in BODIPY dyads: a combined computational and experimental study
Distance dependence of enhanced intersystem crossing in BODIPY-nitroxide dyads
Enhancing Phototoxicity in BODIPY‐Perylene Charge Transfer Dyads by Combined Iodination and Mesylation
Light‐Induced Charge Separation in Covalently Linked BODIPY‐Quinone‐Alkyne Dyads
Light‐Induced Charge Separation in Covalently Linked BODIPY‐Quinone‐Alkyne Dyads
Benefits of using BODIPY–porphyrin dyads for developing deep-red lighting sources
Triplet Formation and Triplet‐Triplet Annihilation Upconversion in Iodine Substituted Non‐Orthogonal BODIPY‐Perylene Dyads
New 8-substituted BODIPY-based chromophores: synthesis, optical and electrochemical properties
Optoelectronic Properties and Fluorescence Lifetime Imaging Application of Donor‐Acceptor Dyads Derived From 2,6‐DicarboxyBODIPY
Unveiling the Ultrafast Excitation Energy Transfer in Tetraarylpyrrolo (3,2‐ b) pyrrole‐BODIPY Dyads
An electrochemical thermal transistor
Halogen‐Bonding Strapped Porphyrin BODIPY Rotaxanes for Dual Optical and Electrochemical Anion Sensing
Solvent and alkyl substitution effects on charge-transfer mediated triplet state generation in BODIPY dyads: a combined computational and experimental study
Distance dependence of enhanced intersystem crossing in BODIPY-nitroxide dyads
Enhancing Phototoxicity in BODIPY‐Perylene Charge Transfer Dyads by Combined Iodination and Mesylation
Light‐Induced Charge Separation in Covalently Linked BODIPY‐Quinone‐Alkyne Dyads
Light‐Induced Charge Separation in Covalently Linked BODIPY‐Quinone‐Alkyne Dyads
Benefits of using BODIPY–porphyrin dyads for developing deep-red lighting sources
Triplet Formation and Triplet‐Triplet Annihilation Upconversion in Iodine Substituted Non‐Orthogonal BODIPY‐Perylene Dyads
New 8-substituted BODIPY-based chromophores: synthesis, optical and electrochemical properties
Optoelectronic Properties and Fluorescence Lifetime Imaging Application of Donor‐Acceptor Dyads Derived From 2,6‐DicarboxyBODIPY
Unveiling the Ultrafast Excitation Energy Transfer in Tetraarylpyrrolo (3,2‐ b) pyrrole‐BODIPY Dyads
An electrochemical thermal transistor
Halogen‐Bonding Strapped Porphyrin BODIPY Rotaxanes for Dual Optical and Electrochemical Anion Sensing