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1361056-20-3

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1361056-20-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1361056-20-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,1,0,5 and 6 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1361056-20:
(9*1)+(8*3)+(7*6)+(6*1)+(5*0)+(4*5)+(3*6)+(2*2)+(1*0)=123
123 % 10 = 3
So 1361056-20-3 is a valid CAS Registry Number.

1361056-20-3Downstream Products

1361056-20-3Relevant academic research and scientific papers

Construction of full-color-tunable and strongly emissive materials by functionalizing a boron-chelate four-ring-fused π-conjugated core

Li, Di,Zhang, Hongyu,Wang, Chenguang,Huang, Shuo,Guo, Jianhua,Wang, Yue

, p. 4319 - 4328 (2012)

2-(2′-Hydroxyphenyl)benzoxazole (HBO) and 2-(2′-hydroxyphenyl) benzothiazole (HBT) reacted with triphenylborane produced two rigid π-conjugated fluorescent cores 1 (BPh2(BOZ), BOZ = 2-(benzo[d]oxazol-2-yl)phenol) and 2 (BPh2(BTZ), BTZ = 2-(benzo[d]thiazol-2-yl)phenol). Comparisons of photophysical properties and calculations between para- and meta-diphenylamine-substituted derivatives 5 (BPh2(para-NPh2-BTZ)) and 7 (BPh2(meta-NPh 2-BTZ)) demonstrated that functionalization at the para-position of the rigid core is effective in tuning the electronic structure and hence the photophysical properties of this type of boron-chelate complex. Simple modification of these frameworks by introducing various amine groups at the para-position allows the synthesis of strongly fluorescent materials 3 (BPh 2(para-Cz-BTZ), Cz = 9H-carbazol-9-yl), 4 (BPh2(para- NPh2-BOZ), NPh2 = diphenylamino), 5, and 6 (BPh 2(para-NMe2-BTZ), NMe2 = dimethylamino). The emission colors of these newly synthesized complexes together with the parent complexes 1 and 2 covered a wide range from deep blue to saturated red in both solution and the solid state. Crystal structure analysis discloses that two phenyl groups attached to the boron atom effectively keep the luminescent ring-fused π-conjugated skeletons apart, making these fluorophores highly emissive in solid forms (ΦF = 0.36-0.71). Organic light-emitting diodes employing these boron complexes as emitters not only keep the full-color tunable emission feature but also show high electroluminescent (EL) performance; for instance, the greenish-blue device based on 2 showed the highest efficiency of 7.8 cd A-1 and the yellow light-emitting device based on 4 exhibited the highest brightness (31220 cd m-2) among the boron-containing emitters reported so far.

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