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TRIS(4 7-DIPHENYL-1 10-PHENANTHROLINE)RU is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

75213-31-9

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75213-31-9 Usage

Uses

Tetramethylrhodamine isothiocyanate mixed isomers is an amino-reactive labeling reagent.

Check Digit Verification of cas no

The CAS Registry Mumber 75213-31-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,2,1 and 3 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 75213-31:
(7*7)+(6*5)+(5*2)+(4*1)+(3*3)+(2*3)+(1*1)=109
109 % 10 = 9
So 75213-31-9 is a valid CAS Registry Number.
InChI:InChI=1/3C24H16N2.2ClHO4.Ru/c3*1-3-7-17(8-4-1)19-13-15-25-23-21(19)11-12-22-20(14-16-26-24(22)23)18-9-5-2-6-10-18;2*2-1(3,4)5;/h3*1-16H;2*(H,2,3,4,5);/q;;;;;+2/p-2

75213-31-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,7-diphenyl-1,10-phenanthroline,ruthenium(2+),diperchlorate

1.2 Other means of identification

Product number -
Other names Tris(4,7-diphenyl-1,10-phenanthroline)ruthenium(II) bis(perchlorate) complex

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:75213-31-9 SDS

75213-31-9Downstream Products

75213-31-9Relevant academic research and scientific papers

Stereochemical Effects on Monolayer Formation of (2+) (dpp = 4,7-Diphenyl-1,10-phenanthroline) at an Air-Water Interface

Yamagishi, Akihiko,Goto, Yasutomo,Taniguchi, Masahiro

, p. 1827 - 1832 (1996)

Stereochemical effects on monolayer formations have been studied at an air-water interface for the racemic mixture and enantiomer of (ClO4)2 (dpp = 4,7-diphenyl-1,10-phenanthroline).Stearic acid (SA) was added to reduce the cohesive interaction of the Ru(II) complexes.The ration of SA to Ru(II) complex, /, was varied from 0 to 4.At / = 0 and 1, the lift-off area per molecule at which the surface pressure increased from zero was smaller for the racemic mixture than for the enantiomer.The results indicated that the racemic mixture of the Ru(II) complex formed a more compact monolayer than the enantiomer.There was no difference observed in the surface pressure-molecular area (?-A) curves at / larger than 3.The monolayer was transferred onto a hydrophobic glass or silicon wafer substrate as a Langmuir-Blodgett (LB) film of Y-type.At / = 1, the d(001) spacing of the film was determined by X-ray diffraction measurements, leading to d(001) = 50.4 and 37.8 Angstroem for the racemic mixture and the enantiomer, respectively.The IR reflection-adsorption spectroscopy showed that the alkyl chains of SA molecules took different orientations for the racemic and enantiomeric films.It is postulated that SA molecules which intervened between the Ru(II) complexes are more perpendicular to the substrate surface due to the closer packing of the racemic Ru(II) complexes than the enantiomers.

Ruthenium(II) Complex as Phosphorescent Dopant for Highly Efficient Red Polymers Light-Emitting Diodes

Xia, Hong,Zhang, Chengbo,Liu, Xiaodong,Qiu, Song,Lu, Ping,Shen, Fangzhong,Zhang, Jingying,Ma, Yuguang

, p. 3185 - 3190 (2004)

Red electrophosphorescence from light-emitting devices based on a ruthenium(II) complex [Ru(4,7-Ph2-phen)3] 2+-doped wide-band-gap semiconductive polymers, e.g., poly(vinylcarbazole) (PVK), polydihexyl-fluorene (PF), and ladder-like polyphenylene (LPPP), as the emitting layer are reported. These polymers show the short-wavelength electroluminescence emission peaking ranged from 410 to 490 nm, which overlaps well with the absorption band of [Ru(4,7-Ph 2-phen)3]2+; however, very efficient energy transfer was investigated in the PVK system, likely due to relative long excited-state lifetimes of PVK than that of PF and LPPP and good chemical compatibility of [Ru(4,7-Ph2-phen)3]2+ with PVK. The EL spectra show the characteristic spectrum of [Ru(4,7-Ph 2-phen)3]2+, with a peak at 612 nm and CIE of (0.62, 0.37) which is comparable with standard red color. The optimized device ITO/PVK 5 wt % [Ru(4,7-Ph2-phen)3]2+/PBD/ Alq3/LiF/Al shows the maximum luminance efficiency and power efficiency of 8.6 cd/A and 2.1 lm/W, respectively.

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