1447947-87-6

Basic information

• Product Name: 2,4,6-tris(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)[1,3,5]triazine
• CAS NO: 1447947-87-6
• Molecular Weight: 687.26
• Mol File: 1447947-87-6.mol

Chemical Properties

• CAS DataBase Reference: 2,4,6-tris(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)[1,3,5]triazine(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4,6-tris(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)[1,3,5]triazine(1447947-87-6)
• EPA Substance Registry System: 2,4,6-tris(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)[1,3,5]triazine(1447947-87-6)

Safety Data

• Hazardous Substances Data: 1447947-87-6(Hazardous Substances Data)

Usage

Uses

Used in Biological Imaging and Labeling:
2,4,6-tris(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)[1,3,5]triazine is used as a fluorescent dye for biological imaging and labeling. Its high photostability and fluorescent quantum yield make it an ideal choice for these applications, allowing for clear and precise visualization of biological processes and structures.
Used in Environmental Sensing:
2,4,6-tris(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)[1,3,5]triazine is also used as a sensor for detecting the presence of harmful chemicals or pollutants in the environment. Its sensitivity and selectivity make it a valuable tool for environmental monitoring and protection.
Used in Organic Light-Emitting Diodes (OLEDs):
2,4,6-tris(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)[1,3,5]triazine has been found to exhibit potential as a material for organic light-emitting diodes and other optoelectronic devices. Its unique optical and electronic properties contribute to the development of advanced display technologies and energy-efficient lighting solutions.
Used in Optoelectronic Devices:
In the field of optoelectronics, 2,4,6-tris(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)[1,3,5]triazine is used as a material for the development of various devices that rely on the interaction of light with electronic components. Its properties make it suitable for applications such as solar cells, photodetectors, and other light-sensitive technologies.

Upstream product

• 61676-62-8 2-Isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 30363-03-2 2,4,6-tris(4-bromophenyl)-1,3,5-triazine 
• 73183-34-3 bis(pinacol)diborane 
• 76347-13-2 2-isopropyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 

Relevant articles and documents

Star-shaped molecule with planar triazine core and perylene diimide branches as an n-type additive for bulk-heterojunction perovskite solar cells

A novel star-shaped molecule, TPDI, featuring a triazine unit as the core and units of a perylene diimide derivative as its conjugated branches, has been synthesized for application as an n-type additive in methylammonium lead iodide (CH3NHsub

Synthesis of pentamethyldisilanyl-substituted starlike molecule with triazine core and its application to dye-sensitized solar cells

Two-dimensional starlike molecule 7 consisting of benzothiadiazole-thiophenylphenyltriazine groups and pentamethyldisilanyl substituted thienylene units that extend to three directions was synthesized by the reactions of 2,4,6-tris[4-(4-hexyl-5-(7-(3-hexy

Solution processable star-shaped molecules with a triazine core and branching thienylenevinylenes for bulk heterojunction solar cells

Two new star-shaped A-π-D molecules with triazine as a core and an acceptor unit, thienylenevinylene as the π bridge, and tert-butyl-substituted triphenylamine (tTPA)- or carbazole (tCz) as the end group and donor units of TTVTPA and TTVCz were synthesized for their application as donor materials in solution processed bulk heterojunction organic solar cells (OSCs). The charge transfer was convergent from peripheral groups to the central core along the conjugated branches in these star-shaped molecules (SSMs). TTVTPA and TTVCz are soluble in common organic solvents. Excellent thermal stability was observed for TTVTPA and TTVCz. OSCs were fabricated by spin-coating a blend of each SSM with the fullerene derivatives (PC61BM or PC71BM) as a composite film-type photoactive layer. The PV properties of the TTVTPA/fullerene derivative based OSCs were considerably better than those of the TTVCz/fullerene derivative blend based OSCs. A power conversion efficiency of 2.48%, a short-circuit current density of 10.57 mA cm-2, an open-circuit voltage of 0.69 V, and a fill factor of 0.34 were observed for the OSC based on the active layer of TTVTPA/PC71BM (1:7, w/w). This journal is

1,3,5-Triazine and dibenzo[: B, d] thiophene sulfone based conjugated porous polymers for highly efficient photocatalytic hydrogen evolution

Organic conjugated porous polymers, triazine-Ph-CPP and triazine-Th-CPP, are synthesized and characterized. Without further addition of co-catalysts, triazine-Ph-CPP exhibits a HER of 16?287 μmol g-1 h-1 and an apparent quantum yield

Engineering the Interconnecting Position of Star-Shaped Donor–π–Acceptor Molecules Based on Triazine, Spirofluorene, and Triphenylamine Moieties for Color Tuning from Deep Blue to Green

Pi-conjugated organic molecules featuring the donor–bridge–acceptor (D–π–A) structure have been widely used in semiconducting materials owing to their rigid structure, good thermal stability, excellent charge transfer, and high emission efficiency. To investigate the effect of the D–π–A molecular structure on the photophysical properties, in this contribution, three star-shaped D–π–A isomers based on the 2,4,6-triphenyl-1,3,5-triazine, spirofluorene, and triphenylamine moieties, that is, p-TFTPA, mp-TFTPA, and m-TFTPA, were synthesized by elaborately engineering the interconnecting position in the building-block units. The optophysical properties of these compounds were systematically explored by experiments and theory calculations. Definitively, changing the interconnecting position in these molecules played a significant role in the degree of π conjugation, which resulted in tunable emission colors from deep blue to green. Moreover, these isomers were employed as emissive dopants in organic light-emitting diodes. The highest external quantum efficiency of 2.3 % and current efficiency of 6.2 cd A?1 were achieved by using the p-TFTPA based device. This research demonstrates a feasible way to realize blue emitters by engineering D–π–A conjugation.