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• 1083009-44-2 2,6-diiodo-4,4-difluoro-1,3,5,7-tetramethyl-8-phenyl-4-bora-3a,4a-diaza-s-indacene 
• 1066-54-2 trimethylsilylacetylene 
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• 1098053-27-0 4,4-difluoro-8-phenyl-2,6-diethynyl-1,3,5,7-tetramethyl-4-bora-3a,4a-diaza-s-indacene 

Relevant academic research and scientific papers

Synthesis and characterization of near-infrared emissive BODIPY-based conjugated polymers

Three novel BODIPY-based conjugated polymers could be synthesized via palladium-catalyzed Sonogashira coupling reaction. Compared with BODIPY model derivatives, the polymers can emit in the range from deep-red to near-infrared region with emission spectral maxima at = 640-660 nm and exhibit moderate fluorescent quantum yield from 0.23 to 0.26. Density functional theory (DFT) calculations are performed on three polymers repeat units, and HOMO and LUMO energy levels of the conjugated polymers are estimated. Georg Thieme Verlag Stuttgart · New York.

Photoresponsiveness of Anthracene-Based Supramolecular Polymers Regulated via a σ-Platinated 4,4-Difluoro-4-bora-3a,4a-diaza- s-indacene Photosensitizer

Anthracene and its derivatives have attracted tremendous interest in recent years because of their intriguing photoresponsive behaviors. Our research group has previously constructed anthracene-based supramolecular polymers, which display multicycle anthracene-endoperoxide photoswitching in a macroscopic manner. However, high-energy light excitation (λ = 365-460 nm) is required for anthracene-to-endoperoxide photooxygenation, giving rise to severe photodegradation problems. In this work, we have developed an effective approach to addressing this issue, by encapsulating a σ-platinated 4,4-difluoro-4-bora-3a,4a-diaza-s-indacene (BODIPY) photosensitizer into anthracene-based supramolecular polymeric systems. The platination effect enhances π-electron delocalization, while promoting intersystem crossing from singlet to triplet excited states. Accordingly, the σ-platinated BODIPY photosensitizer displays excellent 1O2 production capability, facilitating anthracene-to-endoperoxide transformation under low-energy irradiation conditions (λ = 520-590 nm). This leads to the breakup of supramolecular polymers and gels, which can be restored at room and elevated temperatures because of the reversible endoperoxide-to-anthracene deoxygenation process. Overall, the rational design of a σ-metalated photosensitizer opens up a new avenue to regulating the photoresponsiveness of supramolecular polymers under mild and nondestructive conditions.

Trans-Bis(alkylphosphine) platinum(ii)-alkynyl complexes showing broadband visible light absorption and long-lived triplet excited states

Heteroleptic trans-bis(alkylphosphine) platinum(ii) bisacetylide complexes Pt-1 and Pt-2 were prepared to achieve broadband absorption of visible light. Two different ethynylBodipy ligands, 2-ethynylBodipy and 2,6-diethynylBodipy or 8-(4′-ethynylphenyl)Bodipy, were used in each complex. Each Bodipy ligand gives strong absorption in the visible spectral region, but at different wavelengths, thus broadband absorption in the visible spectral region was achieved for the Pt(ii) complexes (ε is up to 1.85 × 105 M-1 cm-1 in the region of 450-700 nm). Singlet energy transfer from the peripheral coordinated Bodipy to the central coordinated Bodipy (with 2,6-diethynyl substitution) was confirmed by steady state absorption/luminescence spectroscopy, fluorescence excitation spectroscopy and nanosecond/femtosecond ultrafast time-resolved transient absorption spectroscopy. Long-lived triplet excited states were observed for both complexes (τT = 63.13 μs for Pt-1 and τT = 94.18 μs for Pt-2). Nanosecond time-resolved transient absorption spectroscopy indicated that the triplet excited state of Pt-1 is distributed on both Bodipy units. For Pt-2, however, the T1 state is confined to the central coordinated Bodipy ligand. These complexes show high singlet oxygen (1O2) quantum yields (ΦΔ = 76.0%). With nanosecond pulsed laser excitation, delayed fluorescence was observed for the complexes (τDF = 43.8 μs for Pt-1 and τDF = 111.0 μs for Pt-2), which is rarely reported for transition metal complexes. The complexes were used as efficient multi-wavelength excitable triplet photosensitizers for triplet-triplet annihilation upconversion. This journal is

Long-lived room-temperature near-IR phosphorescence of BODIPY in a visible-light-harvesting N^C^N PtII-acetylide complex with a directly metalated BODIPY chromophore

Room-temperature long-lived near-IR phosphorescence of boron-dipyrromethene (BODIPY) was observed (λem=770 nm, φP=3.5%, τP=128.4 μs). Our molecular-design strategy is to attach PtII coordination centers directly

Unprecedented laser action from energy transfer in multichromophoric BODIPY cassettes

A cassette molecule, featuring direct integration of two donor BODIPY units to one acceptor BODIPY unit, was conveniently developed as the first highly "through-bond energy transfer" (TBET) laser dye. This multicolor absorbing dye exhibited highly efficie