Category: 638-45-9

Wang, Long published the artcileHigh-Lying 3¹Ag Dark-State-Mediated Singlet Fission, Recommanded Product: 1-Iodohexane, the publication is Journal of the American Chemical Society (2021), 143(15), 5691-5697, database is CAplus and MEDLINE.

Singlet fission (SF), the conversion of one high-energy singlet to two low-energy triplets, provides the potential to increase the efficiency of photovoltaic devices. In the SF chromophores with C_2h symmetry, exemplified by polyenes, singlet-to-triplet conversion generally involves a low-lying 2¹A_g dark state, which serves as either a multiexciton (ME) intermediate to promote the SF process or a parasitic trap state to shunt excited-state populations via internal conversion. This controversial behavior calls for a deep understanding of dark-state-related photophysics involving the higher-lying singlet state. However, the optical “dark” and “transient” nature of these dark states and strong correlation feature of double exciton species make their characterization and interpretation challenging from both exptl. and computational perspectives. In the present work combining transient spectroscopy and multireference electronic structure calculations (XDW-CASPT2), we addressed a new photophys. model, i.e., a high-lying 3¹Ag dark-state-mediated ultrafast SF process in the benzodipyrrolidone (BDPP) skeleton. Such a 3¹Ag dark state with distinctive double excitation character, described as the ME state, could be populated from the initial 1¹Bu bright state on an ultrafast time scale given the quasi-degeneracy and intersection of the two electronic states. Furthermore, the suitable optical band gap and triplet energy, high triplet yield, and excellent photostability render BDPP a promising SF candidate for photovoltaic devices. These results not only enrich the arsenal of SF materials but also shed new insights into the understanding of dark-state-related photophysics, which could promote the development of new SF-active materials.

Journal of the American Chemical Society published new progress about 638-45-9. 638-45-9 belongs to iodides-buliding-blocks, auxiliary class Iodide,Aliphatic hydrocarbon chain, name is 1-Iodohexane, and the molecular formula is C7H13NO2, Recommanded Product: 1-Iodohexane.

Referemce:
https://en.wikipedia.org/wiki/Iodide,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

Fang, Lingyi published the artcileA triple helicene based molecular semiconductor characteristic of a fully fused conjugated backbone for perovskite solar cells, Formula: C6H13I, the publication is Energy & Environmental Science (2022), 15(4), 1630-1637, database is CAplus.

We herein report a triple helicene based mol. semiconductor (TBPC-611), characteristic of a fully fused conjugated backbone containing multiple pyrrole rings. TBPC-611 can be solution-processed with nonvolatile 4-tert-butylpyridinium bis(trifluoromethanesulfonyl)imide into a morphol. heat-resistant composite thin film which also possesses high elec. conductivity and high hole mobility. These combined quality factors allow for its use as the protective hole-transport layer of PSCs with 22.1%-efficiency which are remarkably stable at 85°C for 2000 h. Joint exptl. and theor. investigations have uncovered the crucial correlation of the permeation of internal and external gaseous mols. with the thermal decomposition of perovskites, shedding light on durable perovskite optoelectronic devices.

Energy & Environmental Science published new progress about 638-45-9. 638-45-9 belongs to iodides-buliding-blocks, auxiliary class Iodide,Aliphatic hydrocarbon chain, name is 1-Iodohexane, and the molecular formula is C6H13I, Formula: C6H13I.

Referemce:
https://en.wikipedia.org/wiki/Iodide,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

Xu, Niansheng published the artcileHelical polycycle molecular semiconductor for durable and efficient perovskite solar cells, Product Details of C6H13I, the publication is ACS Materials Letters (2022), 4(1), 11-20, database is CAplus.

Despite the efficiency comparable to crystalline silicon photovoltaics, it is still a severe concern on the long-term stability under the stress of heat, light, and bias potential for perovskite solar cell (PSC). Here, we report a triple aza[6]helicene-based mol. semiconductor (TBTA[6]H) characteristic of a fully fused conjugated backbone. TBTA[6]H presents superior solubility and glass-transition temperature (T_g). An air-doped composite of TBTA[6]H with a high elec. conductivity of 353μS cm^-1 is still featured by a T_g of 112°C, enabling the fabrication of 22% efficiency, 85°C durable PSCs. The TBTA[6]H composite not only exhibits an excellent morphol. stability at 85°C in PSCs, but also remarkably attenuates the thermal degradation of photoactive perovskite layer. The cell with TBTA[6]H also displays an excellent operation stability under the continuous full sunlight soaking at 55°C.

ACS Materials Letters published new progress about 638-45-9. 638-45-9 belongs to iodides-buliding-blocks, auxiliary class Iodide,Aliphatic hydrocarbon chain, name is 1-Iodohexane, and the molecular formula is C7H3ClN2O3, Product Details of C6H13I.

Referemce:
https://en.wikipedia.org/wiki/Iodide,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

Zhang, Linfeng published the artcileMicrowave-Assisted Nickel-Catalyzed Rapid Reductive Coupling of Ethyl 3-iodopropionate to Adipic Acid, Recommanded Product: 1-Iodohexane, the publication is Catalysis Letters (2021), 151(8), 2339-2345, database is CAplus.

3-Iodopropionic acid (3-IPA) can be efficiently synthesized from the glycerol derivative glyceric acid (GA), which is a potential biomaterial-based platform mol. In this report, Et 3-iodopropionate was rapidly dimerized to di-Et adipate in a microwave reactor using NiCl₂.6H₂O as a catalyst, co-catalyzed by Mn and the 1, 10-Phenanthroline monohydrate ligand. Under the optimum reaction conditions, di-Et adipate can be obtained with 84% yield at 90°C in just 5 min. Di-Et adipate was hydrolyzed to obtain the adipic acid (AA) in 89% yield with an acid catalyst. AA is an important chem. and a monomer for producing a wide range of high-performance polymeric substances. This rapid coupling method is also applicable to other alkyl halides.

Catalysis Letters published new progress about 638-45-9. 638-45-9 belongs to iodides-buliding-blocks, auxiliary class Iodide,Aliphatic hydrocarbon chain, name is 1-Iodohexane, and the molecular formula is C18H12ClNO, Recommanded Product: 1-Iodohexane.

Referemce:
https://en.wikipedia.org/wiki/Iodide,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

Xie, Li published the artcileDetermination of hypochlorite and bisulfite in water by bifunctional colorimetric sensor based on octupolar conjugated merocyanine dyes, Quality Control of 638-45-9, the publication is Microchemical Journal (2022), 172(Part_A), 106931, database is CAplus.

In this study, we developed a bifunctional colorimetric fluorescent sensor based on three merocyanine structures for the detection of hypochlorite (ClO^–) and bisulfite (HSO₃^–). In MeOH solution and under special conditions, this sensor shows high selectivity on fluorescence and UV-Vis spectra for the detection of ClO^– and HSO₃^–, resp. The sensor solution exhibits a strong red fluorescence emission at 638 nm, which was quenched and the blue color turned to purple pink rapidly upon the addition of ClO^–. The mechanism of the detection of ClO^– was confirmed via ESI-MS that the C=C groups were induced to produce ethylene oxide and ethylene glycol derivatives by hypochlorite. The fluorescence emission at 638 nm in the concentration range of ClO^– from 0 to 24 μM showed a good linear relationship (R² = 0.9919), and the LOD of the sensor for ClO^– was 0.42 μM. Interestingly, the sensor can also detect HSO₃^– in acid condition (pH less than 7.4). The blue shift of UV-Vis spectra of the solution of sensor were observed after addition of HSO₃^– and irradiation with visible light for about 4 min. The HSO₃^– concentration showed a good linear relationship (R² = 0.9987) at 275 nm in the range of 12-42 μM, and thus its LOD was calculated to be 1.14 μM. Finally, the sensor has important value for detecting ClO^– and HSO₃^– in tap water and lake water.

Microchemical Journal published new progress about 638-45-9. 638-45-9 belongs to iodides-buliding-blocks, auxiliary class Iodide,Aliphatic hydrocarbon chain, name is 1-Iodohexane, and the molecular formula is C9H5ClO2, Quality Control of 638-45-9.

Referemce:
https://en.wikipedia.org/wiki/Iodide,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

Ai, Han-Jun published the artcileRuthenium pincer complex-catalyzed heterocycle compatible alkoxycarbonylation of alkyl iodides: substrate keeps the catalyst active, Name: 1-Iodohexane, the publication is Chemical Science (2022), 13(8), 2481-2486, database is CAplus and MEDLINE.

In this work, a pincer ruthenium pincer complex-catalyzed heterocycle compatible alkoxycarbonylation of alkyl iodides using alcs. and carbon monoxide to afford esters I [R = iPr, tBu, Ph, etc.; R¹ = tBu, cyclopentyl, (CH₂)₃Ph, etc.] was reported. Benefitting from the pincer ligand, a variety of heterocycles, such as thiophenes, morpholine, unprotected indoles, pyrrole, pyridine, pyrimidine, furan, thiazole, pyrazole, benzothiadiazole, and triazole, were compatible in this protocol.

Chemical Science published new progress about 638-45-9. 638-45-9 belongs to iodides-buliding-blocks, auxiliary class Iodide,Aliphatic hydrocarbon chain, name is 1-Iodohexane, and the molecular formula is C6H13I, Name: 1-Iodohexane.

Referemce:
https://en.wikipedia.org/wiki/Iodide,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

Wang, Xiao-Xu published the artcileNiH-catalyzed reductive hydrocarbonation of enol esters and ethers, Recommanded Product: 1-Iodohexane, the publication is CCS Chemistry (2022), 4(2), 605-615, database is CAplus.

Chiral dialkyl carbinols and their derivatives are significant synthetic building blocks in organic chem. and related fields. The development of convenient and efficient methods to access these compounds has long been an important endeavor. Herein, authors report a NiH-catalyzed reductive hydroalkylation and hydroarylation of enol esters and ethers. α-Oxoalkyl organonickel species were generated in situ in a catalytic mode and then participated in cross-coupling with alkyl or aryl halides. This approach enabled C(sp3)-C(sp3) and C(sp3)-C(sp2) bond formation under mild reductive conditions with simple operations, thereby boosting a broad substrate scope and good functional compatibility. Esters of enantioenriched dialkyl carbinols were accessed in a catalytic asym. version. Mechanistic studies demonstrated that this reaction proceeded through a syn-addition of Ni-H intermediate to an enol ester with high regio- and enantioselectivity.

CCS Chemistry published new progress about 638-45-9. 638-45-9 belongs to iodides-buliding-blocks, auxiliary class Iodide,Aliphatic hydrocarbon chain, name is 1-Iodohexane, and the molecular formula is C10H12F6N4O6PdS2, Recommanded Product: 1-Iodohexane.

Referemce:
https://en.wikipedia.org/wiki/Iodide,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

Chen, Bo published the artcileVisible-light-induced defluorinative carbonylative coupling of alkyl iodides with α-trifluoromethyl substituted styrenes, Category: iodides-buliding-blocks, the publication is Organic & Biomolecular Chemistry (2022), 20(26), 5264-5269, database is CAplus and MEDLINE.

A visible-light-mediated defluorinative carbonylative cross-coupling of alkyl iodides RI (R = Me, cyclopentyl, N-Boc azetidin-3-yl, etc.) with α-trifluoromethyl styrenes R¹C(=CH₂)CF₃ (R¹ = 4-benzyloxyphenyl, 3-methylphenyl, 2-naphthyl, etc.) has been developed. The reaction occurs at room temperature under blue light irradiation, and various gem-difluoroalkenes R¹C(CH₂C(O)R)=CF₂ were obtained in moderate to good yields. Synthetic transformations of the obtained product were performed as well.

Organic & Biomolecular Chemistry published new progress about 638-45-9. 638-45-9 belongs to iodides-buliding-blocks, auxiliary class Iodide,Aliphatic hydrocarbon chain, name is 1-Iodohexane, and the molecular formula is C6H13I, Category: iodides-buliding-blocks.

Referemce:
https://en.wikipedia.org/wiki/Iodide,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

Wang, Zhuo published the artcile4-Aminobenzotriazole (ABTA) as a removable directing group for palladium-catalyzed aerobic oxidative C-H olefination, SDS of cas: 638-45-9, the publication is Organic Letters (2022), 24(17), 3107-3112, database is CAplus and MEDLINE.

4-Aminobenzotriazole (ABTA) was applied as an effective removable directing group (DG) in Pd-catalyzed C-H activation for the first time. Compared with the widely applied pyridine and quinoline analogs, ABTA showed significantly improved reactivity, achieving aerobic oxidative C-H olefination in excellent yields (up to 95% vs <50% with other reported DGs under identical conditions). Using this new strategy, macrocyclization was achieved to give cyclic peptides in good yields with easy ABTA removal under mild conditions, highlighting the promising potential of this new DG.

Organic Letters published new progress about 638-45-9. 638-45-9 belongs to iodides-buliding-blocks, auxiliary class Iodide,Aliphatic hydrocarbon chain, name is 1-Iodohexane, and the molecular formula is C7H6Cl2, SDS of cas: 638-45-9.

Referemce:
https://en.wikipedia.org/wiki/Iodide,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

Deuker, Marius published the artcileTetraorganylargentate(III) Complexes: Key Intermediates in Silver-Mediated Cross-Coupling Reactions, COA of Formula: C6H13I, the publication is Organometallics (2021), 40(14), 2354-2363, database is CAplus.

The use of silver as a catalyst in cross-coupling reactions remains underdeveloped. Authors show by electrospray-ionization mass spectrometry that the diorganylargentates LiAgR’₂·Li(CN) (R’ = Me, Bu) formed in situ react with a wide scope of alkyl and aryl halides RX to afford the tetraorganylargentate(III) complexes R’₃AgR^–. Upon fragmentation in the gas phase, these high-valent species readily undergo reductive elimination. The trimethylorganylargentates Me₃AgR^– furnish the synthetically desired cross-coupling products MeR with high selectivity, whereas the tributylorganylargentates Bu₃AgR^– yield more of the homocoupling product Bu₂. Quantum chem. calculations reproduce the exptl. observed trends in reactivity and moreover provide insight into the structures and energetics of the species involved. Their findings indicate that the facile formation of tetraorganylargentate complexes and their high tendency toward reductive elimination can be exploited for the development of silver-mediated cross-coupling reactions as a viable alternative to established synthetic methods.

Organometallics published new progress about 638-45-9. 638-45-9 belongs to iodides-buliding-blocks, auxiliary class Iodide,Aliphatic hydrocarbon chain, name is 1-Iodohexane, and the molecular formula is C6H13I, COA of Formula: C6H13I.

Referemce:
https://en.wikipedia.org/wiki/Iodide,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com