71935-21-2

Upstream product

• 717881-64-6 4-(9H-carbazole-9-yl)benzoic acid ethyl ester 
• 51934-41-9 4-iodobenzoic acid ethyl ester 
• 86-74-8 9H-carbazole 
• 1194-02-1 4-fluorobenzonitrile 
• 57103-17-0 N-(4-cyanophenyl)carbazole 
• 619-58-9 4-iodobenzoic acid 
• 57103-16-9 4-carbazol-9-yl-benzoic acid methyl ester 
• 110677-45-7 N-(4-formylphenyl)carbazole 

Downstream Products

• 937269-48-2 (triphenylphosphine)2Ag(4-carbazol-9-yl-benzoic acid-H) 
• 937269-45-9 Ag(4-carbazol-9-yl-benzoic acid-H) 

Relevant academic research and scientific papers

Zirconium(IV) metallocavitands as blue-emitting materials

A series of zirconium-carboxylate metallocavitands with the general formula [(CpZr)3(μ-κ2,O′,O″CR) 3(μ3-O)(μ2-OH)3]Cl (Cp = cyclopentadienyl; R = C5H4N (5), C6/s

Carbazole-modified thiazolo[3,2-: C] [1,3,5,2]oxadiazaborinines exhibiting aggregation-induced emission and mechanofluorochromism

Two highly emissive carbazole-containing thiazole-fused oxadiazaborinines were designed and synthesized. These N,O-chelated organoboron dyes displayed large Stokes shifts and remarkable solvatofluorochromism in solutions, as well as good thermal stability

Hydrogen bonding boosted the persistent room temperature phosphorescence of pure organic compounds for multiple applications

Persistent room temperature phosphorescence (p-RTP) of pure organic compounds is drawing much attention due to its unique advantages and promising applications in anticounterfeiting, encryption, bioimaging, etc. Achieving efficient p-RTP, however, remains

Synthesis of Small-Molecule/DNA Hybrids through On-Bead Amide-Coupling Approach

Small molecule/DNA hybrids (SMDHs) have been considered as nanoscale building blocks for engineering 2D and 3D supramolecular DNA assembly. Herein, we report an efficient on-bead amide-coupling approach to prepare SMDHs with multiple oligodeoxynucleotide

Electrosynthesis and electrochromic properties of poly(amide-triarylamine)s containing triptycene units

Four bis(amide-triarylamine) derivatives featuring a triptycene as an interior core and terminal electroactive triphenylamine (TPA) or N-phenylcarbazole (NPC) groups were prepared by the condensation reactions from 1,4-bis(4-aminophenoxy)triptycene with 4-carboxytriphenylamine and N-(4-carboxyphenyl)carbazole, respectively, and from 1,4-bis(4-carboxyphenoxy)triptycene with 4-aminotriphenylamine and N-(4-aminophenyl)carbazole, respectively. The electrochemistry and electropolymerization of these bis(amide-triarylamine) derivatives were investigated. The stability of the oxidized forms of the bis(amide-triarylamine)s is affected by the orientation of amide linkage and the structure of terminal triarylamine unit. Two of the bis(amide-triarylamine)s could be electropolymerized into robust films on the electrode surface in an electrolyte solution. The electrogenerated polymer films exhibited reversible electrochemical oxidation processes and strong color changes upon electro-oxidation, which can be switched by potential modulation. The electrochromic properties of the films were evaluated by the spectroelectrochemical and electrochromic switching studies. The TPA-based film showed better electrochromic performance than the NPC-based one.

Effect of self-assembled monolayer treated zno on the photovoltaic properties of inverted polymer solar cells

Inverted bulk hetero-junction polymer solar cells (iPSC) composed of P3HT/PC61BM blends on the ZnO modified with benzoic acid derivatives-based self-assembled monolayers (SAM) are fabricated. Compared with the device using the pristine ZnO, the devices wi