4-4-difluoro-4-bora-3a-4a-diaza-s-indacene and benzothiazole

4-4-difluoro-4-bora-3a-4a-diaza-s-indacene has been researched along with benzothiazole* in 1 studies

Other Studies

1 other study(ies) available for 4-4-difluoro-4-bora-3a-4a-diaza-s-indacene and benzothiazole

Article	Year
AIE-active organoboron complexes with highly efficient solid-state luminescence and their application as gas sensitive materials. Dalton transactions (Cambridge, England : 2003), 2015, Aug-21, Volume: 44, Issue:31 Complexation of a boron atom with two of benzothiazole-enolate-based bidentate ligands successfully gave rise to the corresponding BF2-/BPh2-chelated complexes (), which could be considered as novel AIE-active organoboron luminophores. These new luminophores exhibited aggregation-induced emission, and a large Stokes shift in solution. In the solid-state, compounds exhibited intense emission with high quantum yields of 0.14-0.43. The photophysical properties and AIE characteristics of these compounds were rationalized through X-ray crystal analysis and theoretical calculations. In addition, compounds and were capable of sensing acidic gas by reversible changes of emission, which may potentially serve as solid-state luminescent sensors for acidic vapors. Topics: Alkenes; Benzothiazoles; Boron Compounds; Crystallography, X-Ray; Drug Design; Gases; Hydrogen-Ion Concentration; Luminescent Measurements; Models, Molecular; Molecular Conformation	2015

Article

Year

AIE-active organoboron complexes with highly efficient solid-state luminescence and their application as gas sensitive materials.

Dalton transactions (Cambridge, England : 2003), 2015, Aug-21, Volume: 44, Issue:31

Complexation of a boron atom with two of benzothiazole-enolate-based bidentate ligands successfully gave rise to the corresponding BF2-/BPh2-chelated complexes (), which could be considered as novel AIE-active organoboron luminophores. These new luminophores exhibited aggregation-induced emission, and a large Stokes shift in solution. In the solid-state, compounds exhibited intense emission with high quantum yields of 0.14-0.43. The photophysical properties and AIE characteristics of these compounds were rationalized through X-ray crystal analysis and theoretical calculations. In addition, compounds and were capable of sensing acidic gas by reversible changes of emission, which may potentially serve as solid-state luminescent sensors for acidic vapors.

Topics: Alkenes; Benzothiazoles; Boron Compounds; Crystallography, X-Ray; Drug Design; Gases; Hydrogen-Ion Concentration; Luminescent Measurements; Models, Molecular; Molecular Conformation

2015