Organic chromophores based on small molecules have attracted considerable attention over the past decades due to their potential applications including organic light-emitting diodes (OLEDs), solar cells, dye lasers, photosensitizers and molecular probes.1 A great variety of organic and organometallic luminescent molecules with different chemical/photophysical properties adapted to specific needs have been reported, and a number of those are also commercially available.
2Metal complexes based on the N-and/or O-donor ligands, have shown promising luminescent properties as efficient EL emitters. Among them, aluminum (III) complex of 8-hydroxyquilonine (Alq3) has been used as a green emitter and one of the stable electron transport materials with high emission efficiency.3 Similarly, zinc (II) complex 4 and boron (III) complex 5 of 8-hydroxyquilonine have been investigated as an EL materials in vapor-deposited films. In general, boron compounds are more stable than corresponding aluminum compounds, and boron difluoride dyes such as boron dipyrromethene (BODIPY) and boron diketonates possess remarkable properties such as large molar extinction coefficients, high fluorescence quantum yields and excellent photostability. 2-(2'-Hydroxyphenyl)benzoxazole (HBO) and 2-(2-hydroxyphenyl)benzothiazole (HBT) are widely studied fluorescent compounds for their fundamental photophysics and as optical probes due to their dual emission via excited state intramolecular proton transfer (ESIPT).7 For example, in nonpolar solvent, absorption and emission peaks of HBT are observed at approximately 350 and 530 nm, respectively. This large Stokes shift is due to ESIPT process that occurs when HBT is photoexcited. We recently reported ESIPT-based optical probe, showing that inhibition of intramolcular hydrogen bond of HBT resulted in preventing ESIPT process, and hypsochromic shift. 8 We reasoned that this unique optical change could be applied to construct blue emitting dye compound, which might have high quantum yield by blocking less efficient ESIPT process. Herein, we report the synthesis and characterization of two new boron complexes, 1 and 2, based on HBO and HBT as potential blue luminescent materials.Boron complexes 1 and 2 were synthesized in one step according to Scheme 1. Commercially available HBO and HBT were reacted with boron trifluoride etherate (BF3·OEt2) in dichloromethane at room temperature to give dyes 1 and 2, in 50% and 92% isolated yields. Boron complexes 1 and 2 exhibited good solubility in common organic solvents such as THF, CH2Cl2, CHCl 3 , toluene, dichloroethane and DMSO. Their structure and purity were confirmed by 1 H and 13 C NMR spectroscopy and HR-MS.Boron complexes 1 and 2 emit an intense deep blue light upon being irradiated by UV light in solution and in the solid state. The excitation and emission maxima for 1 and 2 in solution and in the solid state are listed in Table S1. Figure 1 illustrates the absorption and emission spectra of 1, 2, HBO, and HBT in CH2Cl2. The UV-visible absorption spectra of d...