Bałczewski Piotr, Kowalska Emilia, Różycka-Sokołowska Ewa, Uznański Paweł, Wilk Joanna, Koprowski Marek, Owsianik Krzysztof, Marciniak Bernard
Functional Materials Synthesis Group, Division of Organic Chemistry, Centre of Molecular and Macromolecular Studies, Polish Academy of Sciences, Sienkiewicza 112, 90-363 Łódź, Poland.
Structural & Material Chemistry Group, Faculty of Science and Technology, Institute of Chemistry, Jan Dlugosz University in Częstochowa, Armii Krajowej 13/15, 42-200 Częstochowa, Poland.
Materials (Basel). 2021 Jun 23;14(13):3506. doi: 10.3390/ma14133506.
While few studies show only symmetrical and poorly mono-SO (n = 0-2) substituted acenes, in this study, we present a synthesis of a new group of unsymmetrical, significantly substituted derivatives, which revealed unique photophysical properties. Both sulfides (S), sulfoxides (SO) and sulfones (SO) showed very high photochemical stabilities, unusual for these groups, during UV-irradiation at 254/365 nm (air O and Ar), which was higher than any found in the literature. For the (S)/(SO) series (254 nm), the stabilities of 80-519 min. (air O and Ar) were found. At 365 nm, stabilities of 124-812 min./(air O) for (S)/(SO) and higher for (SO) were observed. Photoluminescence lifetimes of (SO) of the lower anthryl symmetry remained in the following order: (SO) < (S) < (SO); those with full symmetry were in the following order: (S) < (SO) < (SO). The enhanced photostability was explained with DFT/MS/Hammett's constants, which showed the leading role of the SO groups in stabilization of HOMO/LUMO frontier orbitals. The SO (n = 0-2) substituted acenes turned out to be tunable violet/blue/green emitters by oxidation of S atoms and the introduction of rich substitution.
虽然很少有研究仅展示对称且单-SO(n = 0 - 2)取代程度低的并苯,但在本研究中,我们报道了一组新型不对称、显著取代衍生物的合成,这些衍生物展现出独特的光物理性质。硫化物(S)、亚砜(SO)和砜(SO₂)在254/365 nm紫外线照射下(空气O₂和Ar)均表现出非常高的光化学稳定性,这对于这些基团来说并不常见,且高于文献中报道的任何值。对于(S)/(SO)系列(254 nm),发现其稳定性为80 - 519分钟(空气O₂和Ar)。在365 nm时,观察到(S)/(SO)的稳定性为124 - 812分钟/(空气O₂),而(SO₂)的稳定性更高。较低蒽基对称性的(SO)的光致发光寿命顺序如下:(SO)<(S)<(SO₂);完全对称的则顺序为:(S)<(SO)<(SO₂)。通过密度泛函理论(DFT)/质谱(MS)/哈米特常数对增强的光稳定性进行了解释,结果表明SO基团在稳定最高占据分子轨道(HOMO)/最低未占据分子轨道(LUMO)前沿轨道方面起主导作用。通过S原子的氧化和引入丰富的取代基,SO(n = 0 - 2)取代的并苯成为了可调节的紫/蓝/绿发光体。