4151-80-8 Usage
Description
4,4'-Biphenyldiboronic acid is a white to light yellow crystal powder, which is a reactant involved in the synthesis of various organic compounds and materials for different applications in the field of electronics and chemistry.
Uses
1. Used in Organic Field-Effect Transistors (OFETs):
4,4'-Biphenyldiboronic acid is used as a reactant for the synthesis of organic semiconductors containing diazaboroles, which are essential components in the fabrication of organic field-effect transistors. These transistors are crucial for the development of flexible and lightweight electronic devices.
2. Used in Cycloparaphenylenes Synthesis:
4,4'-Biphenyldiboronic acid is utilized as a reactant in the synthesis of cycloparaphenylenes via Suzuki coupling. Cycloparaphenylenes are significant molecules in the field of materials science, as they possess unique electronic and optical properties.
3. Used in 1,3,2-Diazaboroine Derivatives:
4,4'-Biphenyldiboronic acid is employed as a reactant in the synthesis of 1,3,2-diazaboroine derivatives, which are vital for the development of organic thin-film transistor applications. These derivatives contribute to the advancement of electronic devices with improved performance and efficiency.
4. Used in Back-to-Back Coupled 2,6-Bis(triazol-1-yl)pyridine Molecules:
4,4'-Biphenyldiboronic acid serves as a reactant in the synthesis of back-to-back coupled 2,6-bis(triazol-1-yl)pyridine molecules. These molecules are essential in the development of novel electronic materials with enhanced properties.
5. Used in Rectangular Host Synthesis:
4,4'-Biphenyldiboronic acid is used as a reactant in the synthesis of rectangular hosts via electrochemical reactions with methylaquacobaloxime and diamine. These hosts are crucial for the development of advanced chemical sensors and molecular recognition systems.
6. Used in Arylboronates Synthesis:
4,4'-Biphenyldiboronic acid is utilized as a reactant in the synthesis of arylboronates from reactions with catechol, dihydroxynaphthalene, and diaminobenzenedithiol. Arylboronates are essential materials for the development of organic field-effect transistors and light-emitting diodes, which are vital components in the electronics industry.
Check Digit Verification of cas no
The CAS Registry Mumber 4151-80-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,1,5 and 1 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 4151-80:
(6*4)+(5*1)+(4*5)+(3*1)+(2*8)+(1*0)=68
68 % 10 = 8
So 4151-80-8 is a valid CAS Registry Number.
4151-80-8Relevant articles and documents
Size-controlled synthesis of conjugated polymer nanoparticles in confined nanoreactors
Deng, Sheng,Zhi, Jian,Zhang, Xianmei,Wu, Qingqing,Ding, Yun,Hu, Aiguo
, p. 14144 - 14148 (2014)
Soluble conjugated polymeric nanoparticles are synthesized by Suzuki-type polycondensation of two monomers (Ax + By, x>2, y≥2) in the channel of ordered mesoporous silica-supported carbon nano-membranes (nanoreactors). These synthesized soluble conjugated microporous polymers (SCMPs) exhibit uniform particle-size distributions and well-controlled particle sizes. The control of particle size stems from the fact that the polycondensations exclusively take place inside the mesochannels of the nano-reactors. Photo-luminescence studies show that polymeric nanoparticles with tetraphenylethene and pyrene substructures are highly fluorescent. The combination of both physical stability and process-ability offered by the soluble polymeric nanoparticles makes them particularly attractive in light emitting and other optoelectronic applications.
Micropatterning of metallopolymers: Syntheses of back-to-back coupled octylated 2,6-Bis(pyrazolyl)pyridine ligands and their solution-processable coordination polymers
Basak, Supratim,Hui, Pramiti,Boodida, Sathyanarayana,Chandrasekar, Rajadurai
experimental part, p. 3620 - 3626 (2012/06/15)
This paper presents a 10-step synthetic route for the preparation of a series of new back-to-back coupled 2,6-bis(pyrazol-1-yl)pyridine (bpp) ligands (L0-L3) decorated with tetraoctyl chains. Ligand L1 self-assembles with Zn 2+ ion to form a highly soluble metallo-supramolecular polymer 1 with Mn ～ 9600 g/mol. To demonstrate the processability of polymer 1, by following a "top-down" approach periodic one-dimensional fluorescent microstripes were fabricated on a silica substrate.
Organic field-effect transistors based on novel organic semiconductors containing diazaboroles
Kojima, Takahiro,Kumaki, Daisuke,Nishida, Jun-Ichi,Tokito, Shizuo,Yamashita, Yoshiro
experimental part, p. 6607 - 6613 (2011/10/19)
New π-conjugated systems containing a diazaborole unit have been prepared by the reaction of the corresponding boronic acids with diamines. They are nearly colorless compounds with electron-donating properties. Single crystal X-ray structure analysis of t
