Aromatic [b]-fused BODIPY dyes as promising near-infrared dyes

J Wang, N Boens, L Jiao, E Hao - Organic & Biomolecular Chemistry, 2020 - pubs.rsc.org
Far-red and near-infrared (NIR) absorbing/emitting dyes have found diverse applications in
biomedicine and material science. However, the absorption and emission of classical …

Red and NIR emitting ring-fused BODIPY/aza-BODIPY dyes

VK Shukla, G Chakraborty, AK Ray, S Nagaiyan - Dyes and Pigments, 2023 - Elsevier
BODIPY dyes are well-known for their outstanding features, such as solubility in a wide
range of solvents, useful photophysical properties, and good photochemical and thermal …

Unveiling the photophysical properties of boron-dipyrromethene dyes using a new accurate excited state coupled cluster method

R Berraud-Pache, F Neese, G Bistoni… - Journal of chemical …, 2019 - ACS Publications
Boron-dipyrromethene (BODIPY) molecules form a class of fluorescent dyes known for their
exceptional photoluminescence properties. Today, they are used extensively in various …

[HTML][HTML] Insight into the Stokes shift, divergent solvatochromism and aggregation-induced emission of boron complexes with locked and unlocked …

M Mas-Montoya, AG Alcaraz, AE Ferao, D Bautista… - Dyes and …, 2023 - Elsevier
Two four-coordinate boron complexes, compounds 5 and 7, have been synthesized, using
analogous benzophenanthridine-based ligands but showing different conformational …

Naphtho [b]-fused BODIPYs: one pot Suzuki–Miyaura–Knoevenagel synthesis and photophysical properties

Z Zhou, J Zhou, L Gai, A Yuan, Z Shen - Chemical Communications, 2017 - pubs.rsc.org
Naphtho [b]-fused BODIPYs have been facilely synthesized via Suzuki–Miyaura–
Knoevenagel reaction between mono-iodo-BODIPY or 2, 6-diiodo-BODIPY with (2 …

Synthesis and characterization of boron difluoride complexes bearing π-expanded pyridine ligands as organic fluorochromes

T Nakano, A Sumida, K Naka - The Journal of Organic Chemistry, 2021 - ACS Publications
Novel boron complexes bearing pyrrole and π-expanded pyridine structures, such as
quinoline, isoquinoline, and phenanthridine, were prepared. These compounds showed the …

Tunable Yellow to Near-Infrared Fluorescent Boron-Amino-Chelating Complexes with Stokes Shifts> 100 nm

J He, X Chang, C Zou, Y Yu, S Han, C Wu… - The Journal of …, 2023 - ACS Publications
A series of diphenylboron-chelating N-substituent 8-aminoquinoline, 5-aminoquinoxaline,
and 1-aminophenazine were prepared. They exhibit lowest energy absorption peaks of 444 …

Synthesis and Semiconducting Characteristics of the BF2 Complexes of Bisbenzothiophene-Fused Azadipyrromethenes

W Sheng, F Chang, Q Wu, E Hao, L Jiao, JY Wang… - Organic …, 2019 - ACS Publications
A novel type of dibenzothiophene [b]-fused core-expanded azaBODIPYs were obtained
through an efficient post-functionalization of tetrabrominated azadipyrromethenes, using CuI …

Tuning the photophysical properties of BODIPY dyes used in DSSCs as predicted by double‐hybrid TD‐DFT: The role of the methyl substituents

W Helal, A Marashdeh, Q Alkhatib… - … Journal of Quantum …, 2022 - Wiley Online Library
A series of 16 BODIPY dye for DSSC applications are designed with the aim of obtaining a
controlled red‐shift of their absorption band maxima. The design is based on changing the …

Aryl/Heteroaryl Substituted Boron-Difluoride Complexes Bearing 2-(Isoquinol-1-yl) pyrrole Ligands Exhibiting High Luminescence Efficiency with a Large Stokes Shift

T Nakano, S Fujikawa - The Journal of Organic Chemistry, 2022 - ACS Publications
A series of 2-(isoquinol-1-yl) pyrrole-boron complexes possessing (hetero) aryl substituents
on the pyrrole and/or isoquinoline moiety were prepared. These compounds exhibited the …