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2,2':6',2''-Terpyridine, 4'-[3,5-bis(1,1-dimethylethyl)phenyl]is a chemical compound that belongs to the terpyridine family. It features a terpyridine core with a 4'-[3,5-bis(1,1-dimethylethyl)phenyl]substitution, which can influence its steric and electronic properties, making it a versatile molecule for various chemical and biological processes.

227948-34-7

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227948-34-7 Usage

Uses

Used in Coordination Chemistry:
2,2':6',2''-Terpyridine, 4'-[3,5-bis(1,1-dimethylethyl)phenyl]is used as a chelating ligand for the formation of metal complexes in coordination chemistry. The terpyridine core and the bulky 3,5-bis(1,1-dimethylethyl)phenyl group attached to it allow for the creation of stable complexes with various metal ions.
Used in Catalysis:
In the field of catalysis, 2,2':6',2''-Terpyridine, 4'-[3,5-bis(1,1-dimethylethyl)phenyl]is used as a ligand to modify the properties of metal catalysts. The steric and electronic effects of the compound can enhance the catalytic activity and selectivity of the metal centers in various chemical reactions.
Used in Material Science:
Used in Medicinal Chemistry:

Check Digit Verification of cas no

The CAS Registry Mumber 227948-34-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,7,9,4 and 8 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 227948-34:
(8*2)+(7*2)+(6*7)+(5*9)+(4*4)+(3*8)+(2*3)+(1*4)=167
167 % 10 = 7
So 227948-34-7 is a valid CAS Registry Number.

227948-34-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(3,5-ditert-butylphenyl)-2,6-dipyridin-2-ylpyridine

1.2 Other means of identification

Product number -
Other names -

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 -
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More Details:227948-34-7 SDS

227948-34-7Relevant academic research and scientific papers

Highly Efficient Ir(III)-Coumarin Photo-Redox Catalyst for Synergetic Multi-Mode Cancer Photo-Therapy

Fan, Zhongxian,Xie, Jiaen,Sadhukhan, Tumpa,Liang, Chao,Huang, Can,Li, Wenqing,Li, Tingxuan,Zhang, Pingyu,Banerjee, Samya,Raghavachari, Krishnan,Huang, Huaiyi

, (2021/12/06)

Four photo-catalysts of the general formula [Ir(CO6/ppy)2(L)]Cl where CO6=coumarin 6 (Ir1–Ir3), ppy=2-phenylpyridine (Ir4), L=4′-(3,5-di-tert-butylphenyl)-2,2′ : 6′,2′′-terpyridine (Ir1), 4′-(3,5-bis(trifluoromethyl)phenyl)-2,2′ : 6′,2′′-terpyr

Synthesis and photophysical properties of iridium(III) bisterpyridine and its homologues: A family of complexes with a long-lived excited state

Collin, Jean-Paul,Dixon, Isabelle M.,Sauvage, Jean-Pierre,Gareth Williams,Barigelletti, Francesco,Flamigni, Lucia

, p. 5009 - 5016 (2007/10/03)

A new synthetic procedure has been developed which makes possible the preparation of IrLL′3+ complexes (L, L′ = terpyridine derivative) in good yields. In a first step, IrLCl3 is obtained under relatively mild conditions as an intermediate. Subsequent reaction with L′ (a few minutes in refluxing ethylene glycol) affords IrLL′3+. The electrochemical behavior and ground- and excited-state spectroscopic properties of four IrLL′3+ complexes in nitrile solvents are reported. The X-ray structure of one of these complexes is also described. The complexes have been designed keeping in mind their incorporation in linearly arranged multicomponent arrays, according to a templating strategy based on the assembly of tpy-type ligands by the Ir(III) center. The complexes feature a high-lying level for the luminescent excited state (>2.5 eV), with a satisfactory room-temperature luminescence intensity (φem ≈ 10-2) and lifetime on the microsecond time scale. These favorable properties indicate that the Ir(III)-tpy center will not be the final recipient of the energy-harvesting processes in multipartite systems built around them. Temperature-dependent studies of the luminescence properties in the 95-298 K range indicate that the higher-lying levels of these complexes are not efficient pathways for deactivation of the luminescent states. For these reasons, it is concluded that the studied Ir-tpy-type complexes are well suited (i) to play the role of photoactive center and to gather photo- and electroactive units or (ii) to act as electron relays in linearly arranged multicomponent arrays.

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