Tag: M.W:300-400

Kim, Chang-Kyu; Nakazawa, Dante; Duhamel, Georges; Raptis, Konstantinos; Ruas, Alexandre published an article about the compound: Tri-n-octylphosphine Oxide( cas:78-50-2,SMILESS:CCCCCCCCP(CCCCCCCC)(CCCCCCCC)=O ).Synthetic Route of C24H51OP. Aromatic heterocyclic compounds can be classified according to the number of heteroatoms or the size of the ring. The authors also want to convey more information about this compound (cas:78-50-2) through the article.

Abstract: A combined method of high-resolution gamma spectroscopy and thermal ionization mass spectroscopy without chem. separation was applied for plutonium assay in pure Pu and U-Pu mixed solutions collected at the Rokkasho Reprocessing Plant, Japan. The relative biases of Pu assay results determined by the combined method to the conventional IDMS are less than 0.01% in the pure Pu and the U-Pu mixed solutions The combined method can be used as an alternative rapid method for Pu assay as a backup to the conventional IDMS method and K-edge densitometry without any loss of precision and accuracy.

From this literature《Improved combined HRGS-TIMS method for rapid determination of Pu in nuclear material samples collected in the Rokkasho reprocessing plant》,we know some information about this compound(78-50-2)Synthetic Route of C24H51OP, but this is not all information, there are many literatures related to this compound(78-50-2).

Reference:
Chapter 1 An introduction to palladium catalysis,
Palladium/carbon catalyst regeneration and mechanical application method

In organic chemistry, atoms other than carbon and hydrogen are generally referred to as heteroatoms. The most common heteroatoms are nitrogen, oxygen and sulfur. Now I present to you an article called Solvent-Controlled Intermolecular Proton-Transfer Follows an Irreversible Eigen-Weller Model from fs to ns, published in 2021-12-31, which mentions a compound: 78-50-2, mainly applied to solvent controlled intermol proton transfer, Name: Tri-n-octylphosphine Oxide.

Intermol. Proton Transfer (PT) dynamics can be best studied by optical spectroscopy, which can cover the vast timescale spanned by the process. PT in a hydrogen bonding complex between a pyranine-based photoacid and a trialkyl-phosphine oxide is addressed. The photoreaction is traced with the help of femtosecond transient absorption and picosecond-resolved fluorescence. Characteristic kinetics and spectra of the intervening species are isolated by global anal. and spectral decomposition of time-resolved fluorescence. It is found that the shared proton shifts towards the phosphine site upon photoexcitation in acetonitrile. The process occurs on the sub-picosecond timescale, essentially, under solvent control. Despite the ultrafast rate, an equilibrium between the complex and the hydrogen-bonded ion pair (HBIP) is established. Further reaction steps are delayed to the nanosecond timescale, where formation of the excited deprotonated form is observed The far-reaching consistency between the various methods supports an irreversible Eigen-Weller mechanism in the excited state.

From this literature《Solvent-Controlled Intermolecular Proton-Transfer Follows an Irreversible Eigen-Weller Model from fs to ns》,we know some information about this compound(78-50-2)Name: Tri-n-octylphosphine Oxide, but this is not all information, there are many literatures related to this compound(78-50-2).

Reference:
Chapter 1 An introduction to palladium catalysis,
Palladium/carbon catalyst regeneration and mechanical application method

Yamamoto, Yoshihiko; Kinpara, Keisuke; Saigoku, Tomoaki; Nishiyama, Hisao; Itoh, Kenji published the article 《Synthesis of benzo-fused lactams and lactones via Ru(ii)-catalyzed cycloaddition of amide- and ester-tethered α,ω-diynes with terminal alkynes: electronic directing effect of internal conjugated carbonyl group》. Keywords: diyne amide linked terminal alkyne regioselective cycloaddition ruthenium; lactam benzo preparation; ester linked diyne terminal alkyne regioselective cycloaddition ruthenium; lactone benzo preparation; cycloaddition catalyst ruthenium.They researched the compound: Chloro(1,5-cyclooctadiene)(pentamethylcyclopentadienyl)ruthenium( cas:92390-26-6 ).Synthetic Route of C18H28ClRu. Aromatic heterocyclic compounds can be divided into two categories: single heterocyclic and fused heterocyclic. In addition, there is a lot of other information about this compound (cas:92390-26-6) here.

In the presence of a catalytic amount of Cp*RuCl(cod), 1,6- and 1,7-diynes connected by an amide or an ester tether underwent cycloaddition with terminal alkynes at room temperature to give rise to cycloadducts, e.g., I, in 40-93% yields with 63 : 37-83 : 17 regioisomer ratios.

Compound(92390-26-6)Synthetic Route of C18H28ClRu received a lot of attention, and I have introduced some compounds in other articles, similar to this compound(Chloro(1,5-cyclooctadiene)(pentamethylcyclopentadienyl)ruthenium), if you are interested, you can check out my other related articles.

Reference:
Chapter 1 An introduction to palladium catalysis,
Palladium/carbon catalyst regeneration and mechanical application method

Related Products of 78-50-2. The fused heterocycle is formed by combining a benzene ring with a single heterocycle, or two or more single heterocycles. Compound: Tri-n-octylphosphine Oxide, is researched, Molecular C24H51OP, CAS is 78-50-2, about Quantitative Electrochemical Control over Optical Gain in Quantum-Dot Solids. Author is Geuchies, Jaco J.; Brynjarsson, Baldur; Grimaldi, Gianluca; Gudjonsdottir, Solrun; van der Stam, Ward; Evers, Wiel H.; Houtepen, Arjan J..

Solution-processed quantum dot (QD) lasers are one of the holy grails of nanoscience. They are not yet commercialized because the lasing threshold is too high: one needs >1 exciton per QD, which is difficult to achieve because of fast nonradiative Auger recombination. The threshold can, however, be reduced by electronic doping of the QDs, which decreases the absorption near the band-edge, such that the stimulated emission (SE) can easily outcompete absorption. Here, by electrochem. doping films of CdSe/CdS/ZnS QDs, the authors achieve quant. control over the gain threshold. The authors obtain stable and reversible doping of more than two electrons per QD. The authors quantify the gain threshold and the charge carrier dynamics using ultrafast spectroelectrochem. and achieve quant. agreement between experiments and theory, including a vanishingly low gain threshold for doubly doped QDs. Over a range of wavelengths with appreciable gain coefficients, the gain thresholds reach record-low values of ~1 × 10-5 excitons per QD. These results demonstrate a high level of control over the gain threshold in doped QD solids, opening a new route for the creation of cheap, solution-processable, low-threshold QD lasers.

Compound(78-50-2)Related Products of 78-50-2 received a lot of attention, and I have introduced some compounds in other articles, similar to this compound(Tri-n-octylphosphine Oxide), if you are interested, you can check out my other related articles.

Reference:
Chapter 1 An introduction to palladium catalysis,
Palladium/carbon catalyst regeneration and mechanical application method

In organic chemistry, atoms other than carbon and hydrogen are generally referred to as heteroatoms. The most common heteroatoms are nitrogen, oxygen and sulfur. Now I present to you an article called Ruthenium-catalyzed synthesis of functionalized dienes from propargylic esters: formal cross-coupling of two carbenes, published in 2009, which mentions a compound: 92390-26-6, mainly applied to conjugated diene stereoselective synthesis; Ruthenium catalyzed cross coupling diazoalkane carbene propargylic ester, Name: Chloro(1,5-cyclooctadiene)(pentamethylcyclopentadienyl)ruthenium.

The coupling of a propargylic ester with a diazoalkane in the presence of [RuCl(cod)Cp*] catalyst leads to the formation of functionalized conjugated dienes with high stereoselectivity. The reaction involves the cross-coupling of a vinylcarbene fragment, arising from a ruthenium-catalyzed propargylic ester rearrangement, with a diazoalkane carbene.

Here is a brief introduction to this compound(92390-26-6)Name: Chloro(1,5-cyclooctadiene)(pentamethylcyclopentadienyl)ruthenium, if you want to know about other compounds related to this compound(92390-26-6), you can read my other articles.

Reference:
Chapter 1 An introduction to palladium catalysis,
Palladium/carbon catalyst regeneration and mechanical application method

Epoxy compounds usually have stronger nucleophilic ability, because the alkyl group on the oxygen atom makes the bond angle smaller, which makes the lone pair of electrons react more dissimilarly with the electron-deficient system. Compound: Tri-n-octylphosphine Oxide, is researched, Molecular C24H51OP, CAS is 78-50-2, about Selective Extraction of Sc(III) over Y(III) and Fe(III) with a Deep Eutectic Solvent Composed of N-Lauroylsarcosine and Tri-n-octylphosphine Oxide.Product Details of 78-50-2.

Demand for scandium (Sc) has been increasing in recent years. However, there are almost no ores containing Sc, and the supply is insufficient because the separation and recovery of Sc as a byproduct from oxide minerals such as ilmenite ore, bauxite, and laterite are difficult. In this study, extraction and separation of Sc3+ from acidic chloride or acidic nitrate solutions containing transition metals such as Fe3+, Co2+, Ni2+, Zn2+, and Pd2+ were studied using N-lauroylsarcosine (NLS) and tri-n-octylphosphine oxide (TOPO), which together create a “”deep eutectic solvent”” (DES). Owing to the resp. selectivity of NLS and TOPO by different extractive interactions between metal ions and the two extractants in toluene, Sc3+ was effectively and selectively separated even from Fe3+ in the aqueous ammonium nitrate solution, the mutual separation of which is difficult with NLS alone. The mutual separation of Sc3+ and Fe3+ in acidic chloride solution is in general very difficult, while the mutual separation of these metals from acidic nitrate solution is successful. This is due to either anions forming complexes with Sc3+ in the aqueous phase (chloride) or not (nitrate). The potential use of the combination of the NLS with TOPO for selective recovery of Sc3+ from Fe3+ in a refining process is demonstrated.

Here is a brief introduction to this compound(78-50-2)Product Details of 78-50-2, if you want to know about other compounds related to this compound(78-50-2), you can read my other articles.

Reference:
Chapter 1 An introduction to palladium catalysis,
Palladium/carbon catalyst regeneration and mechanical application method

Recommanded Product: Chloro(1,5-cyclooctadiene)(pentamethylcyclopentadienyl)ruthenium. The fused heterocycle is formed by combining a benzene ring with a single heterocycle, or two or more single heterocycles. Compound: Chloro(1,5-cyclooctadiene)(pentamethylcyclopentadienyl)ruthenium, is researched, Molecular C18H28ClRu, CAS is 92390-26-6, about Synthesis of 2-Alkoxy-5-methylenetetrahydropyrans: A Regioselective Ruthenium-Catalyzed C-C Coupling Reaction of Prop-2-yn-1-ols with Allyl Alcohol. Author is Derien, Sylvie; Ropartz, Loiec; Le Paih, Jacques; Dixneuf, Pierre H..

The carbon-carbon coupling of prop-2-yn-1-ols with allyl alc. is achieved in the presence of the ruthenium(II) catalyst RuCl(cod)(C5Me5). The coupling reaction is highly regioselective and leads to the HOCR2C(:CH2)CH2CH2CHO isomer and, after cyclization, to either 2-hydroxy- or 2-alkoxy-5-methylenetetrahydropyrans, at room temperature or at 80 °C, resp. It is used for the synthesis of mols. containing two and three tetrahydropyran moieties. The study of a variety of prop-2-yn-1-ols has shown the influence of the substituent at the propargyl carbon on the regioselectivity of the C-C coupling. In the case of tertiary alcs., the reaction leads to only one cyclic isomer, the 2-alkoxytetrahydropyran whereas with secondary alcs., a linear isomer is also obtained. The tetrahydropyranols are easily oxidized into lactones.

Here is a brief introduction to this compound(92390-26-6)Recommanded Product: Chloro(1,5-cyclooctadiene)(pentamethylcyclopentadienyl)ruthenium, if you want to know about other compounds related to this compound(92390-26-6), you can read my other articles.

Reference:
Chapter 1 An introduction to palladium catalysis,
Palladium/carbon catalyst regeneration and mechanical application method

Application In Synthesis of Tri-n-octylphosphine Oxide. The fused heterocycle is formed by combining a benzene ring with a single heterocycle, or two or more single heterocycles. Compound: Tri-n-octylphosphine Oxide, is researched, Molecular C24H51OP, CAS is 78-50-2, about Membrane support formulation and carrier selection in supported liquid membrane for extraction of zwitterionic form of Glutamic acid. Author is Rajendaren, Vikneswary; Saufi, Syed M.; Zahari, M. A. K. M.; Mohammad, Abdul Wahab.

Glutamic acid (GA) is an amino acid which is usually appear in the zwitterionic form in solutions At present, cation and anion exchange carriers are widely use to extract this amino acids. However, the carriers only function either at high pH or low pH. Although, the pH can be adjusted by adding certain chem. to reach acidic or basic region, but it may lead to addnl. byproducts formation and affect the extraction process. In the current study, supported liquid membrane (SLM) was used to extract the zwitterionic form of GA from the aqueous solution without any pH adjustment. In the SLM process, the determination of the best carrier in liquid membrane formulation is important for achieving high extraction of GA. Hence, different types of carriers such as trioctylamine (TOA), tridodecylamine (TDA), tri-n-octyl phosphine oxide (TOPO), mixture of 50% TOA and 50% TDA, aliquat 336 and di-2-ethylhexyl phosphoric acid (D2EHPA) in 2-ethyl-1-hexanol were investigated. The polyethersulfone (PES) membrane with and without graphene membrane supports were prepared, characterized and used as the support in the SLM. The incorporation of graphene in PES membrane had increased the surface contact angle and tensile stress from 80.96 ± 1.92° to 97.8 ± 1.46° and 650.684 kPa to 1079.59 kPa, resp. Aliquat 336 was identified as the best carrier with 93% of GA extraction

Here is a brief introduction to this compound(78-50-2)Application In Synthesis of Tri-n-octylphosphine Oxide, if you want to know about other compounds related to this compound(78-50-2), you can read my other articles.

Reference:
Chapter 1 An introduction to palladium catalysis,
Palladium/carbon catalyst regeneration and mechanical application method

Computed Properties of C24H51OP. Aromatic compounds can be divided into two categories: single heterocycles and fused heterocycles. Compound: Tri-n-octylphosphine Oxide, is researched, Molecular C24H51OP, CAS is 78-50-2, about Shape Evolution and Control of Wurtzite CdSe Nanocrystals through a Facile One-Pot Strategy. Author is Zhang, Haoran; Cao, Zetan; He, Jia; Liu, Zhiwen; Peng, Simin; Liu, Xi; Chen, Bin.

The synthesis of one-dimensional (1D) CdSe nanocrystals (NCs) with hexagonal wurtzite (WZ) structures such as nanorods has been well developed over the past years. However, the shape modulation of WZ-CdSe with two-dimensional (2D)/three-dimensional (3D) morphologies remains challenging because of its intrinsic hexagonal unit and the involved ligands selectively binding to specific crystal facets. Here, we present a facile and general one-pot approach for the shape control of WZ-CdSe NCs without using pre-existing seeds. Interestingly, the low supersaturation in a drip injection mode enabled the control and formation of various shapes including the nanorods, long nanowires, and hexagonal platelets, compared to the traditional one-time injection. Such shape evolutions could be conveniently tuned by the parameters such as the temperature, growth time, and injection rates. The underlying growth mechanisms for the morphol. evolution and control were discussed in the context of kinetic/thermodn. factors. Our studies provide a fundamental understanding of shape modulations in polytypic compound NCs, offering great opportunities to tune the shape-size-property relationship for optoelectronic applications.

Here is a brief introduction to this compound(78-50-2)Computed Properties of C24H51OP, if you want to know about other compounds related to this compound(78-50-2), you can read my other articles.

Reference:
Chapter 1 An introduction to palladium catalysis,
Palladium/carbon catalyst regeneration and mechanical application method

Application of 78-50-2. Aromatic heterocyclic compounds can also be classified according to the number of heteroatoms contained in the heterocycle: single heteroatom, two heteroatoms, three heteroatoms and four heteroatoms. Compound: Tri-n-octylphosphine Oxide, is researched, Molecular C24H51OP, CAS is 78-50-2, about Electrical Tuning of Optical Properties of Quantum Dot-Graphene Hybrid Devices: Interplay of Charge and Energy Transfer. Author is Dutta, Riya; Kakkar, Saloni; Mondal, Praloy; Chauhan, Neha; Basu, J. K..

The combination of semiconductor quantum dots (QD) and single-layer graphene (SLG) can lead to the formation of optoelectronic devices with enhanced sensitivity and can have extensive applications in the field of the photodetector and photovoltaics. The optical properties of the resultant hybrid material are controlled by the interplay of energy transfer between QDs and charge transfer between the QDs and SLG. By studying the steady-state and time-resolved photoluminescence spectroscopy of hybrid QD-SLG devices, we observe a subtle interplay of short- and long-range energy transfer between cadmium selenide (CdSe) QDs in a compact monolayer solid film placed in close proximity to an SLG and the charge transfer from the QD solid to SLG. At larger separation, δ, between the compact monolayer QD and SLG, the emission properties are dominated by mutual energy transfer between the QDs. At relatively smaller separation the emission from QDs, which is strongly quenched, is dominated by charge transfer between QDs and SLG. In addition, we are also able to tune the relative strength of energy and charge transfer by electrostatic doping through the back gate voltage, which provides a novel pathway to tune emission properties of these devices for possible applications as photodetectors, in photovoltaics, and for sensing.

Here is a brief introduction to this compound(78-50-2)Application of 78-50-2, if you want to know about other compounds related to this compound(78-50-2), you can read my other articles.

Reference:
Chapter 1 An introduction to palladium catalysis,
Palladium/carbon catalyst regeneration and mechanical application method