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Push-pull dioxaborine as fluorescent molecular rotor: far-red fluorogenic probe for ligand-receptor interactions

Journal of materials chemistry. C, Materials for optical and electronic devices, 2016-04, Vol.4 (14), p.32-39

2016

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Preparation of Viscosity-Sensitive Isoxazoline/Isoxazolyl-Based Molecular Rotors and Directly Linked BODIPY–Fulleroisoxazoline from the Stable meso-(Nitrile Oxide)-Substituted BODIPY

Organic letters, 2019-07, Vol.21 (14), p.5713-5718

2019

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Flexible BODIPY Platform That Offers an Unexpected Regioselective Heterocyclization Reaction toward Preparation of 2‑Pyridone[a]‑Fused BODIPYs

Journal of organic chemistry, 2019-02, Vol.84 (4), p.2133-2147

2019

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NIR absorbing diferrocene-containing meso-cyano-BODIPY with a UV-Vis-NIR spectrum remarkably close to that of magnesium tetracyanotetraferrocenyltetraazaporphyrin

Chemical communications (Cambridge, England), 2016-01, Vol.52 (77), p.11563-11566

2016

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Boradipyrromethenecyanines

European Journal of Organic Chemistry, 2009-07, Vol.2009 (19), p.3237-3243

2009

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3,5-Bis(acetaldehyde) substituted BODIPY

Organic & biomolecular chemistry, 2013-02, Vol.11 (5), p.835-841

2013

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Anionic, cationic and merocyanine polymethine dyes based on dipyrromethene core

Dyes and pigments, 2013-07, Vol.98 (1), p.113-118

2013

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α-Polymethine-Substituted Boron Dipyrromethenes - BODIPY-Based NIR Cyanine-Like Dyes

European Journal of Organic Chemistry, 2012-03, Vol.2012 (9), p.1825-1834

2012

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Boradipyrromethenecyanines of different electronic symmetry: A demonstration of the potential of BODIPY nucleus as end group in polymethine chromophoric system

Dyes and pigments, 2014-07, Vol.106, p.161-167

2014

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An efficient method of chemical modification of BODIPY core

Tetrahedron, 2013-03, Vol.69 (10), p.2233-2238

2013

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A sensing mechanism for the detection of carbon nanotubes using selective photoluminescent probes based on ionic complexes with organic dyes

Light, science & applications, 2016-02, Vol.5 (2), p.e16028-e16028

2016

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NIR absorbing diferrocene-containing meso-cyano-BODIPY with a UV-Vis-NIR spectrum remarkably close to that of magnesium tetracyanotetraferrocenyltetraazaporphyrinElectronic supplementary information (ESI) available: Selected spectroscopic properties, DFT data, and a detailed experimental procedure for the preparation of 4. CCDC 1494012. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c6cc06344f

2016-09

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3,5-Bis(acetaldehyde) substituted BODIPYElectronic supplementary information (ESI) available: These data include copies of 1H and 13C NMR spectra for all compounds. See DOI: 10.1039/c2ob27004h

2013-01

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Boradipyrromethenecyanines on the base of a BODIPY nucleus annelated with a pyridone ring: a new approach to long-wavelength dual fluorescent probe design

RSC advances, 2013-01, Vol.3 (46), p.24193

2013

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(4,4-Difluoro-4-bora-3a,4a,-diaza-s-indacen-3-yl)acetaldehyde: Synthesis and chemical properties

Journal of heterocyclic chemistry, 2009-11, Vol.46 (6), p.1386-1391

2009

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ChemInform Abstract: (4,4-Difluoro-4-bora-3a,4a-diaza-s-indacen-3-yl)acetaldehyde: Synthesis and Chemical Properties

ChemInform, 2010-04, Vol.41 (16), p.no-no

2010

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Push-pull dioxaborine as fluorescent molecular rotor: far-red fluorogenic probe for ligand-receptor interactions

Preparation of Viscosity-Sensitive Isoxazoline/Isoxazolyl-Based Molecular Rotors and Directly Linked BODIPY–Fulleroisoxazoline from the Stable meso-(Nitrile Oxide)-Substituted BODIPY

Flexible BODIPY Platform That Offers an Unexpected Regioselective Heterocyclization Reaction toward Preparation of 2‑Pyridone[a]‑Fused BODIPYs

NIR absorbing diferrocene-containing meso-cyano-BODIPY with a UV-Vis-NIR spectrum remarkably close to that of magnesium tetracyanotetraferrocenyltetraazaporphyrin

Boradipyrromethenecyanines

3,5-Bis(acetaldehyde) substituted BODIPY

Anionic, cationic and merocyanine polymethine dyes based on dipyrromethene core

α-Polymethine-Substituted Boron Dipyrromethenes - BODIPY-Based NIR Cyanine-Like Dyes

Boradipyrromethenecyanines of different electronic symmetry: A demonstration of the potential of BODIPY nucleus as end group in polymethine chromophoric system

An efficient method of chemical modification of BODIPY core

A sensing mechanism for the detection of carbon nanotubes using selective photoluminescent probes based on ionic complexes with organic dyes

3,5-Bis(acetaldehyde) substituted BODIPYElectronic supplementary information (ESI) available: These data include copies of 1H and 13C NMR spectra for all compounds. See DOI: 10.1039/c2ob27004h

Boradipyrromethenecyanines on the base of a BODIPY nucleus annelated with a pyridone ring: a new approach to long-wavelength dual fluorescent probe design

(4,4-Difluoro-4-bora-3a,4a,-diaza-s-indacen-3-yl)acetaldehyde: Synthesis and chemical properties

ChemInform Abstract: (4,4-Difluoro-4-bora-3a,4a-diaza-s-indacen-3-yl)acetaldehyde: Synthesis and Chemical Properties

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