Tag: 500-600

Golestanzadeh, Mohsen et al. published their research in ChemistrySelect in 2019 | CAS: 96761-85-2

3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl (cas: 96761-85-2) belongs to organobromine compounds. Bromo compounds are employed in a variety of metal-catalyzed coupling reactions. They are also ideal candidates for the synthesis of Grignard reagents that have wide-applicability in organic synthesis. One prominent application of synthetic organobromine compounds is the use of polybrominated diphenyl ethers as fire-retardants, and in fact fire-retardant manufacture is currently the major industrial use of the element bromine.Formula: C24H15Br3

Effect of Confined Spaces in the Catalytic Activity of 1D and 2D Heterogeneous Carbon-Based Catalysts for Synthesis of 1,3,5-Triarylbenzenes: RGO-SO3H vs. MWCNTs-SO3H was written by Golestanzadeh, Mohsen;Naeimi, Hossein. And the article was included in ChemistrySelect in 2019.Formula: C24H15Br3 This article mentions the following:

One hot debate between catalytic activities of sulfonated reduced graphene oxide (RGO-SO3H), as the 2D heterogeneous carbon-based catalyst, and sulfonated multi-walled carbon nanotubes (MWCNTs-SO3H), as the 1D heterogeneous carbon-based catalyst, was investigated in the synthesis of 1,3,5-triarylbenzenes under different conditions. This comparison study revealed that the 2D catalytic system was more efficient relative to the 1D catalyst in terms of yields of the target products, turnover frequency of the catalyst (TOF), and the reusability. The reasons of this observation such as sp. surface area, confinement spaces in 1D and 2D carbon-based catalysts, solvent accessible surface area, surface active sites, and the availability of supported functional groups on carbon nanostructures will discuss. Moreover, the application of synthesized compounds as a substrate was checked in carbon-carbon bond formation. Also, one of the synthesized compounds was produced using three approaches under metal and non-metal conditions. Notably, the recyclability of the two catalytic systems was checked. In the experiment, the researchers used many compounds, for example, 3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl (cas: 96761-85-2Formula: C24H15Br3).

3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl (cas: 96761-85-2) belongs to organobromine compounds. Bromo compounds are employed in a variety of metal-catalyzed coupling reactions. They are also ideal candidates for the synthesis of Grignard reagents that have wide-applicability in organic synthesis. One prominent application of synthetic organobromine compounds is the use of polybrominated diphenyl ethers as fire-retardants, and in fact fire-retardant manufacture is currently the major industrial use of the element bromine.Formula: C24H15Br3

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Jang, Seokhoon et al. published their research in Synthetic Metals in 2018 | CAS: 96761-85-2

3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl (cas: 96761-85-2) belongs to organobromine compounds. Organo bromine compounds are versatile compounds and are widely used in diverse fields. Organo bromine derivatives are used in the dye sector, as an indicator in analytical chemistry (Bromothymol blue is a popular indicator). The reactivity of organobromine compounds resembles but is intermediate between the reactivity of organochlorine and organoiodine compounds. For many applications, organobromides represent a compromise of reactivity and cost.Name: 3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl

Pyrimidine based hole-blocking materials with high triplet energy and glass transition temperature for blue phosphorescent OLEDs was written by Jang, Seokhoon;Han, Si Hyun;Lee, Jun Yeob;Lee, Youngu. And the article was included in Synthetic Metals in 2018.Name: 3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl This article mentions the following:

New hole-blocking materials (HBMs), mPyrPPB and pPPyrPB, consisting of pyrimidine and phenylene segments for high-performance blue phosphorescent OLEDs were designed and synthesized. The thermal, electrochem., and optical properties of mPyrPPB and pPPyrPB were systemically studied. The Tg values of mPyrPPB and pPPyrPB were 118 and 137°, resp. The triplet energy and HOMO energy level of mPyrPPB were 2.77 eV and -6.86 eV, resp., indicating that it had sufficiently high triplet energy and deep HOMO energy level for the hole-blocking layer (HBL) in blue phosphorescent OLED devices. All the meta conjugation of mPyrPPB mol. structure effectively prevented π-electron delocalization and thus increased the triplet energy and electron transport property. MPyrPPB exhibited higher electron-transporting property than pPPyrPB because mPyrPPB possessed effective intermol. H bonds. When mPyrPPB was used as a HBM for a blue phosphorescent OLED device, external quantum efficiency (EQE), current efficiency (CE), and power efficiency (PE) values effectively increased to 16.4%, 36.7 cd/A, and 13.4 lm/W, resp. Compared to the reference device without HBM, EQE, CE, and PE increased by 38%, 35%, and 54%, resp., mainly due to the confinement of triplet excitons and holes and improved electron-transporting ability. In the experiment, the researchers used many compounds, for example, 3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl (cas: 96761-85-2Name: 3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl).

3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl (cas: 96761-85-2) belongs to organobromine compounds. Organo bromine compounds are versatile compounds and are widely used in diverse fields. Organo bromine derivatives are used in the dye sector, as an indicator in analytical chemistry (Bromothymol blue is a popular indicator). The reactivity of organobromine compounds resembles but is intermediate between the reactivity of organochlorine and organoiodine compounds. For many applications, organobromides represent a compromise of reactivity and cost.Name: 3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Su, Shi-Jian et al. published their research in Advanced Materials (Weinheim, Germany) in 2008 | CAS: 96761-85-2

3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl (cas: 96761-85-2) belongs to organobromine compounds. Most of the natural organobromine compounds are produced by marine organisms, and several brominated metabolites with antibacterial, antitumor, antiviral, and antifungal activity have been isolated from seaweed, sponges, corals, molluscs, and others. In the pharmaceutical industry organo bromine derivatives are used as sedatives, vasodilators, antiseptic agents, and anticancer agents.SDS of cas: 96761-85-2

Pyridine-containing triphenylbenzene derivatives with high electron mobility for highly efficient phosphorescent OLEDs was written by Su, Shi-Jian;Chiba, Takayuki;Takeda, Takashi;Kido, Junji. And the article was included in Advanced Materials (Weinheim, Germany) in 2008.SDS of cas: 96761-85-2 This article mentions the following:

Two pyridine-containing triphenylbenzene derivatives of 1,3,5-tri(m-pyrid-3-yl-phenyl)benzene (TmPyPB) and 1,3,5-tri(p-pyrid-3-yl-phenyl)benzene (TpPyPB) with high electron mobility and high triplet energy level are designed and synthesized. Highly efficient blue and green phosphorescent OLEDs are achieved by using TmPyPB and TpPyPB as an electron-transport layer, resp. In the experiment, the researchers used many compounds, for example, 3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl (cas: 96761-85-2SDS of cas: 96761-85-2).

3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl (cas: 96761-85-2) belongs to organobromine compounds. Most of the natural organobromine compounds are produced by marine organisms, and several brominated metabolites with antibacterial, antitumor, antiviral, and antifungal activity have been isolated from seaweed, sponges, corals, molluscs, and others. In the pharmaceutical industry organo bromine derivatives are used as sedatives, vasodilators, antiseptic agents, and anticancer agents.SDS of cas: 96761-85-2

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Midya, Siba P. et al. published their research in Organic Letters in 2022 | CAS: 96761-85-2

3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl (cas: 96761-85-2) belongs to organobromine compounds. A variety of minor organobromine compounds are found in nature, but none are biosynthesized or required by mammals. Organobromine compounds have fallen under increased scrutiny for their environmental impact. Commercially available organobromine pharmaceuticals include the vasodilator nicergoline, the sedative brotizolam, the anticancer agent pipobroman, and the antiseptic merbromin. Recommanded Product: 96761-85-2

Room-Temperature Synthesis of 1,3,5-Tri(het)aryl Benzene from Nitroalkenes Using Pd(OAc)2: Complete Mechanistic and Theoretical Studies was written by Midya, Siba P.;Mondal, Subal;Islam, Abu S. M.;Rashid, Ambreen;Mondal, Sahidul;Paul, Ankan;Ghosh, Pradyut. And the article was included in Organic Letters in 2022.Recommanded Product: 96761-85-2 This article mentions the following:

Herein, a room-temperature catalytic pathway for 1,3,5-tri(het)aryl benzene derivatives I [R = Ph, 4-MeC6H4, 4-ClC6H4, etc.] via Pd(OAc)2-catalyzed cascade cyclotrimerization of nitroalkenes was presented. This newly developed C-C bond-forming methodol. takes place in a cascade manner with the initial pallado-Morita-Baylis-Hillman (MBH) type adduct. The broad substrate scopes, functional group tolerance, and different aryl-substituted benzene derivatives made this methodol. more attractive. Furthermore, the mechanistic understanding through isolation of intermediates and DFT studies of the catalytic cycle provide requisite insight into the methodol. In the experiment, the researchers used many compounds, for example, 3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl (cas: 96761-85-2Recommanded Product: 96761-85-2).

3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl (cas: 96761-85-2) belongs to organobromine compounds. A variety of minor organobromine compounds are found in nature, but none are biosynthesized or required by mammals. Organobromine compounds have fallen under increased scrutiny for their environmental impact. Commercially available organobromine pharmaceuticals include the vasodilator nicergoline, the sedative brotizolam, the anticancer agent pipobroman, and the antiseptic merbromin. Recommanded Product: 96761-85-2

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Iyer, Vivekanantan S. et al. published their research in Angewandte Chemie, International Edition in English in 1997 | CAS: 96761-85-2

3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl (cas: 96761-85-2) belongs to organobromine compounds. Organo bromine compounds are versatile compounds and are widely used in diverse fields. Organo bromine derivatives are used in the dye sector, as an indicator in analytical chemistry (Bromothymol blue is a popular indicator). The reactivity of organobromine compounds resembles but is intermediate between the reactivity of organochlorine and organoiodine compounds. For many applications, organobromides represent a compromise of reactivity and cost.Name: 3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl

From hexa-peri-hexabenzocoronene to “superacenes” was written by Iyer, Vivekanantan S.;Wehmeier, Mike;Brand, J. Diedrich;Keegstra, Menno A.;Mullen, Klaus. And the article was included in Angewandte Chemie, International Edition in English in 1997.Name: 3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl This article mentions the following:

The polyphenylene I was prepared and characterized. Intramol. cyclodehydration of I with AlCl3 and copper triflate in CS2 afforded a black solid, which gave a broad mass spectral peak in the mass range expected for the analogous C222 graphite unit. In the experiment, the researchers used many compounds, for example, 3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl (cas: 96761-85-2Name: 3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl).

3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl (cas: 96761-85-2) belongs to organobromine compounds. Organo bromine compounds are versatile compounds and are widely used in diverse fields. Organo bromine derivatives are used in the dye sector, as an indicator in analytical chemistry (Bromothymol blue is a popular indicator). The reactivity of organobromine compounds resembles but is intermediate between the reactivity of organochlorine and organoiodine compounds. For many applications, organobromides represent a compromise of reactivity and cost.Name: 3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Yang, Kai et al. published their research in Organic Letters in 2021 | CAS: 96761-85-2

3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl (cas: 96761-85-2) belongs to organobromine compounds. Organo bromine compounds are versatile compounds and are widely used in diverse fields. Organo bromine derivatives are used in the dye sector, as an indicator in analytical chemistry (Bromothymol blue is a popular indicator). The reactivity of organobromine compounds resembles but is intermediate between the reactivity of organochlorine and organoiodine compounds. For many applications, organobromides represent a compromise of reactivity and cost.COA of Formula: C24H15Br3

Hydrogen-Bonding Controlled Nickel-Catalyzed Regioselective Cyclotrimerization of Terminal Alkynes was written by Yang, Kai;Wang, Pengfei;Sun, Ze-Ying;Guo, Minjie;Zhao, Wentao;Tang, Xiangyang;Wang, Guangwei. And the article was included in Organic Letters in 2021.COA of Formula: C24H15Br3 This article mentions the following:

Herein a hydrogen-bonding controlled nickel-catalyzed regioselective cyclotrimerization of terminal alkynes in moderate to excellent yields with high regioselectivities toward 1,3,5-trisubstituted benzenes is reported. This method features a cheap catalyst, mild reaction conditions, and excellent functional group compatibility. The Ni-B(OH)2 complex in situ generated from NiCl2·DME and tetrahydroxydiboron might act as an active catalyst. After three consecutive cis-additions of terminal alkynes, internal migratory insertion cyclization, and β-boron elimination induced aromatization, 1,3,5-trisubstituted benzenes were selectively established. In the experiment, the researchers used many compounds, for example, 3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl (cas: 96761-85-2COA of Formula: C24H15Br3).

3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl (cas: 96761-85-2) belongs to organobromine compounds. Organo bromine compounds are versatile compounds and are widely used in diverse fields. Organo bromine derivatives are used in the dye sector, as an indicator in analytical chemistry (Bromothymol blue is a popular indicator). The reactivity of organobromine compounds resembles but is intermediate between the reactivity of organochlorine and organoiodine compounds. For many applications, organobromides represent a compromise of reactivity and cost.COA of Formula: C24H15Br3

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Schulz, Wolfgang W. et al. published their research in Anal. Chem. in 1963 | CAS: 96761-85-2

3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl (cas: 96761-85-2) belongs to organobromine compounds. Many of the organo bromine compounds are relatively nonpolar. Bromine is more electronegative than carbon (2.8 vs 2.5) and hence the carbon in a carbon–bromine bond is electrophilic in nature. Many of the alkyl bromine derivatives are excellent alkylating agents since bromides are good leaving groups. Tribromides, like tetrabutylammonium tribromide, are used as a solid source of bromine. N-bromosuccimide (NBS) is used for the selective bromination of allylic bonds.SDS of cas: 96761-85-2

Separation of stereoisomers by column fractional precipitation was written by Schulz, Wolfgang W.;Purdy, William C.. And the article was included in Anal. Chem. in 1963.SDS of cas: 96761-85-2 This article mentions the following:

Column fractional precipitation is extended to the separation of 1,3,5-tris(3-bromophenyl)benzene from 1,3,5-tris(4-bromophenyl)benzene, with p-dioxane-water. The 3 fractions of greatest overlap were analyzed from the absorbances at 260.2 and 253.0 mμ by using simultaneous equations. o,p-Quaterphenyl was separated from m,p-quaterphenyl and the overlapping fractions were analyzed by the absorbance ratios at 265 and 248 mμ. In the experiment, the researchers used many compounds, for example, 3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl (cas: 96761-85-2SDS of cas: 96761-85-2).

3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl (cas: 96761-85-2) belongs to organobromine compounds. Many of the organo bromine compounds are relatively nonpolar. Bromine is more electronegative than carbon (2.8 vs 2.5) and hence the carbon in a carbon–bromine bond is electrophilic in nature. Many of the alkyl bromine derivatives are excellent alkylating agents since bromides are good leaving groups. Tribromides, like tetrabutylammonium tribromide, are used as a solid source of bromine. N-bromosuccimide (NBS) is used for the selective bromination of allylic bonds.SDS of cas: 96761-85-2

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Noland, Wayland E. et al. published their research in Synthetic Communications in 2019 | CAS: 96761-85-2

3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl (cas: 96761-85-2) belongs to organobromine compounds. Organo bromine compounds are versatile compounds and are widely used in diverse fields. Organo bromine derivatives are used in the dye sector, as an indicator in analytical chemistry (Bromothymol blue is a popular indicator). In the pharmaceutical industry organo bromine derivatives are used as sedatives, vasodilators, antiseptic agents, and anticancer agents.Computed Properties of C24H15Br3

Condensation of 2-methylindole with acetophenones: An unexpected formation of 2-arylanilines was written by Noland, Wayland E.;Novikov, Alexei V.;Brown, Christopher D.. And the article was included in Synthetic Communications in 2019.Computed Properties of C24H15Br3 This article mentions the following:

2-Methylindole condenses with acetophenones under acidic conditions to produce 2-arylanilines in moderate to good yields. The reaction proceeds well with a range of 3′- and 4′- substituted acetophenones (fluoro-, chloro-, bromo-, iodo-, Me, methoxy), and select 2′- substituted ones (fluoro-, methoxy-). No products were obtained with nitro- substitution in any position. In the experiment, the researchers used many compounds, for example, 3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl (cas: 96761-85-2Computed Properties of C24H15Br3).

3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl (cas: 96761-85-2) belongs to organobromine compounds. Organo bromine compounds are versatile compounds and are widely used in diverse fields. Organo bromine derivatives are used in the dye sector, as an indicator in analytical chemistry (Bromothymol blue is a popular indicator). In the pharmaceutical industry organo bromine derivatives are used as sedatives, vasodilators, antiseptic agents, and anticancer agents.Computed Properties of C24H15Br3

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Liu, Xiaoning et al. published their research in Angewandte Chemie, International Edition in 2021 | CAS: 96761-85-2

3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl (cas: 96761-85-2) belongs to organobromine compounds. Most of the natural organobromine compounds are produced by marine organisms, and several brominated metabolites with antibacterial, antitumor, antiviral, and antifungal activity have been isolated from seaweed, sponges, corals, molluscs, and others. Many of the alkyl bromine derivatives are excellent alkylating agents since bromides are good leaving groups. Tribromides, like tetrabutylammonium tribromide, are used as a solid source of bromine. N-bromosuccimide (NBS) is used for the selective bromination of allylic bonds.Application of 96761-85-2

Single-Handed Double Helix and Spiral Platelet Formed by Racemate of Dissymmetric Cages was written by Liu, Xiaoning;Shi, Zheng;Xie, Mingchen;Xu, Jianping;Zhou, Zhifan;Jung, Sinyeong;Cui, Guijia;Zuo, Yong;Li, Tao;Yu, Chunyang;Liu, Zhiqiang;Zhang, Shaodong. And the article was included in Angewandte Chemie, International Edition in 2021.Application of 96761-85-2 This article mentions the following:

Spontaneous deracemization has been used to sep. homochiral domains from the racemic system. However, homochirality can only be referred to when the scales of these domains and systems are specified. To clarify this, we report self-assembly of racemates of dissym. cages DC-1 (I) with a cone-shape propeller geometry, forming a centrosym. columnar crystalline phase (racemic at crystallog. level). Owing to their anisotropic geometry, the two enantiomers are packed in a frustrated fashion in this crystalline phase; single-handed double helixes are observed (single-handedness at supramol. level). The frustrated packing (layer continuity break-up) in turn facilitates screw dislocation during the crystal growth, forming left- or right-handed spiral platelets (symmetry-breaking at morphol. level), although each platelet is composed of DC-1 racemates. The symmetry correlation between DC-1 mols., the crystalline phase and spiral platelets, all exhibit C3 symmetry. In the experiment, the researchers used many compounds, for example, 3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl (cas: 96761-85-2Application of 96761-85-2).

3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl (cas: 96761-85-2) belongs to organobromine compounds. Most of the natural organobromine compounds are produced by marine organisms, and several brominated metabolites with antibacterial, antitumor, antiviral, and antifungal activity have been isolated from seaweed, sponges, corals, molluscs, and others. Many of the alkyl bromine derivatives are excellent alkylating agents since bromides are good leaving groups. Tribromides, like tetrabutylammonium tribromide, are used as a solid source of bromine. N-bromosuccimide (NBS) is used for the selective bromination of allylic bonds.Application of 96761-85-2

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Lu, Tingting et al. published their research in Dyes and Pigments in 2018 | CAS: 96761-85-2

3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl (cas: 96761-85-2) belongs to organobromine compounds. Organo bromine compounds are versatile compounds and are widely used in diverse fields. Organo bromine derivatives are used in the dye sector, as an indicator in analytical chemistry (Bromothymol blue is a popular indicator). Bromine-containing agents predominate because not only are they more efficient than similar chlorine-containing species, but also the high atomic weight of bromine ensures that it is present in a high mass fraction within most organobromine compounds.Category: bromides-buliding-blocks

Reduced efficiency roll-off and enhanced excition confinement in exciplex-type host: Electron transport materials based on benzimidazole units was written by Lu, Tingting;Jiang, Wei;Sun, Kaiyong;Tian, Wenwen;Sun, Yueming. And the article was included in Dyes and Pigments in 2018.Category: bromides-buliding-blocks This article mentions the following:

Two high triplet energy electron transporting materials, tris(3-(1H-benzo[d]imidazol-2-yl)phenyl)benzene (BMZ-TB) and tris(3-(1H-benzo[d]imidazol-2-yl)phenyl)triazine (BMZ-TZ), were successfully designed and synthesized by Suzuki coupling reaction to form efficient exciplexes with the commonly used hole-transporting mols., 4,4′,4”-tris[3-methylphenyl(phenyl)amino]-triphenylamine (m-MTDATA), 1,1-bis[4-[N,N-di(p-tolyl)-amino]phenyl]-cyclohexane (TAPC) and tris(4-carbazoyl-9-ylphenyl)-amine (TCTA). The optical, electrochem., thermal and device properties of BMZ-TB and BMZ-TZ were systematically characterized. In comparison, Ir(mppy)3 based device host with TCTA:BMZ-TZ had high performance, showing a very low efficiency roll-off with the current efficiency of 24.9 cd A-1 at 1000 cd m-2, 23.7 cd A-1 at 5000 cd m-2, and 22.0 cd A-1 at 10000 cd m-2. Furthermore, systematic study of the excited-state dynamics found that the excessively high or low triplet energy of exciplex would induce a serious energy leakage from the complex state to the constituting mol. or from guest material to the exciplex state. In the experiment, the researchers used many compounds, for example, 3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl (cas: 96761-85-2Category: bromides-buliding-blocks).

3,3”-Dibromo-5′-(3-bromophenyl)-1,1′:3′,1”-terphenyl (cas: 96761-85-2) belongs to organobromine compounds. Organo bromine compounds are versatile compounds and are widely used in diverse fields. Organo bromine derivatives are used in the dye sector, as an indicator in analytical chemistry (Bromothymol blue is a popular indicator). Bromine-containing agents predominate because not only are they more efficient than similar chlorine-containing species, but also the high atomic weight of bromine ensures that it is present in a high mass fraction within most organobromine compounds.Category: bromides-buliding-blocks

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary