Category: 1111-67-7

While the job of a research scientist varies, most chemistry careers in research are based in laboratories, where research is conducted by teams following scientific methods and standards. 1111-67-7, Name is Cuprous thiocyanate, belongs to copper-catalyst compound, is a common compound. Reference of 1111-67-7In an article, once mentioned the new application about 1111-67-7.

Coordination position isomers of the type (PPh3)2Co(NCS)2Cu2(SCN)2 and Co(NCS)2(PPh3)2Cu2(SCN)2 and their adducts of the type (xL)Co(NCS)2(PPh3)2Cu2(SCN)2 have been synthesized and studied on the basis of elemental analyses, molar conductance, magnetic susceptibility measurements, infrared and electronic spectral studies.

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Reference：
Copper catalysis in organic synthesis – NCBI,
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

In chemical reaction engineering, simulations are useful for investigating and optimizing a particular reaction process or system. Synthetic Route of 1111-67-7, Name is Cuprous thiocyanate, Synthetic Route of 1111-67-7, molecular formula is CCuNS. In a article，once mentioned of Synthetic Route of 1111-67-7

Cuprous oxide (Cu2O) nanowire films were in situ grown from pre-deposited cuprous thiocyanate (CuSCN) films which acted as sacrificial precursors. The synthesis was processed in air from NaOH solution, providing an appealing alternative to nanowire-based porous films. Plausible solid-liquid interface reactions were described. Structural analysis showed that Cu 2O nanowires were p-type polycrystalline semiconductor, with high aspect ratio of 10-30 nm in diameter and more than 1 um in length, and they were found to be interlaced with each other in the formation of interpenetrating networks within the Cu2O film which possessed large-area uniformity. It is noteworthy that the nanowire-based films actually are porous films embedded with various interwire spaces and cavities. Photoelectrochemical measurements revealed that a Cu2O film with thickness of 500-1000 nm generated zero-bias photocurrent of approximately 1.5 muA cm-2. The present synthesis is facile and low-cost, and is expected to be suitable for mass production of large-area semiconductor films under ambient condition.

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Reference：
Copper catalysis in organic synthesis – NCBI,
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

Modeling chemical reactions helps engineers virtually understand the chemistry, optimal size and design of the system, and how it interacts with other physics that may come into play. category: copper-catalyst. Introducing a new discovery about 1111-67-7, Name is Cuprous thiocyanate

The present invention provides complexes of the formula(L)M(X),in which M is a metal atom selected from copper,silver and gold;L is a carbene ligand; and X is a monoanionic ligand. The complexes are useful as light emitters in the emissive zone of light-emitting devices such as OLEDs. The present invention also provides organometallic complexes which exhibit RASI photoemission, and the use of the same in light-emitting devices such as OLEDs.

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Reference：
Copper catalysis in organic synthesis – NCBI,
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

In chemical reaction engineering, simulations are useful for investigating and optimizing a particular reaction process or system. Electric Literature of 1111-67-7, Name is Cuprous thiocyanate, Electric Literature of 1111-67-7, molecular formula is CCuNS. In a article，once mentioned of Electric Literature of 1111-67-7

Several new complexes of the type [Cu(NO3)(PPh3)2(L)m] (L=3-methylpyrazole, 4-methylpyrazole, 3,5-dimethylpyrazole, 4-bromopyrazole or bis(4-methylpyrazol-1-yl)methane, m=1; L=pyrazole, 1,2,4-triazole or 2-methylimidazole, m=2), [Cu(NO3)(PPh3)(L)] (L=3,4,5-trimethylpyrazole or 4-phenylimidazole), [Cu(NO)3(PAr3)n(L)3] (Ar=p- or m-tolyl, n=0 or 1, L=pyrazole),[CuX(PPh3)2(L)] (X=Cl, Br or I, L=pyrazole or 3,5-dimethylpyrazole) and [CuX(PPh3)(L)] (X=Cl or Br, L=bis(pyrazol-1-yl)methane, bis(3,5-dimethy lpyrazol-1-yl)methane or bis(triazol-1-yl)methane) have been prepared and characterized by analytical and spectral data. The compounds [CuX(PPh3)(L)] (X=Cl, Br or I, L=pyrazole or 3,5-dimethylpyrazole) are fluxional at temperature above 240 K. The dinuclear compound [Cu2(PPh3)3(pzH)2] was obtained when the reaction between [CuI(PPh3)3] and pyrazole (pzH) wascarried out in methanol containing alkali. In the crystal structure of the title compound, the copper atom is found in a strongly distorted tet rahedral coordination [P-Cu-P: 128.0(1)°] with two long Cu-O distances [2.217(9) and 2.184(9) A].

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Reference：
Copper catalysis in organic synthesis – NCBI,
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

The prevalence of solvent effects in heterogeneous catalysis in condensed media has motivated developing quantitative kinetic, and theoretical assessments of solvent structures and their interactions with reaction intermediates and transition states. 1111-67-7, Name is Cuprous thiocyanate, belongs to copper-catalyst compound, is a common compound. Related Products of 1111-67-7In an article, once mentioned the new application about 1111-67-7.

An ambient pressure superconductivity of (BEDT-TTF)2Cu(SCN)2 was observed by d.c. magnetic susceptibility and electrical conductivity measurements.The superconducting critical temperature is the highest (Tc=10.4 K) among the organic superconductors so far obtained, even though the anion has a positional disorder in the crystal.

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Reference：
Copper catalysis in organic synthesis – NCBI,
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

Having gained chemical understanding at molecular level, chemistry graduates may choose to apply this knowledge in almost unlimited ways, as it can be used to analyze all matter and therefore our entire environment. 1111-67-7, Name is Cuprous thiocyanate, belongs to copper-catalyst compound, is a common compound. Synthetic Route of 1111-67-7In an article, once mentioned the new application about 1111-67-7.

The reaction of Kpmf (pmf = anion of N,N?-bis(pyrimidyl-2-yl) formamidine, Hpmf) with CuSCN afforded the complexes K[Cu4(pmF) 3(SCN)2], 1, and Cu4(pmf)4, 2. Reaction of 1 with [(n-Bu)4N]PF6 in THF gave the complex [(n-Bu)4N][Cu4(pmf)3(SCN)2], 3. Their structures were characterized by X-ray crystallography. Complexes 1 and 3 are the first linear tetranuclear complexes containing only Cu(I) atoms, while complex 2 is cyclic. The four Cu(I) atoms of complexes 1 and 3 are helically bridged by three tetradentate pmf- ligands. The [Cu 4(pmf)3(SCN)2]- anions of 1 show weak interactions with adjacent [K(THF)5]+ cations through the sulfur atoms, forming infinite chains which are subjected to a series of intermolecular pi-pi interactions. In complex 2, the pmf- ligands are coordinated to the copper atoms in bidentate fashion through the two central amine nitrogen atoms, leaving the pyrimidine nitrogen atoms uncoordinated. Unexpected fluxional behaviors were observed for complexes 1 and 3 in solution. By the DNMR analysis, the free energy of activation (DeltaGc?) for the exchange is 12.8 kcal mol-1 at 278 K (Tc), and the rate constant of exchange (Kc) is 470 s-1 for 1. The DeltaGc? and Kc are 12.6 kcal mol-1 at 273 K and 433 s-1, respectively, for 3. The Royal Society of Chemistry 2005.

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Reference：
Copper catalysis in organic synthesis – NCBI,
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

When developing chemical systems it’s of course important to gain a deep understanding of the chemical reaction process. Computed Properties of CCuNS, Name is Cuprous thiocyanate, Computed Properties of CCuNS, molecular formula is CCuNS. In a article，once mentioned of Computed Properties of CCuNS

Organolead trihalide perovskite materials have attracted considerable interest because of their successful application in fabricating high-efficiency photovoltaic cells. Charge transport layers play a significant role in improving the efficiency and stability of perovskite solar cells (PSCs). In this work, we investigated the p-type doping effect of the poly(triarylamine) (PTAA) layer on the performance of PSCs by using three dopants. We observe that doping copper(I) thiocyanate (CuSCN) into PTAA led to a higher performance improvement for the PSCs than the use of copper(I) iodide (CuI) or lithium salt (Li-TFSI) as the dopant. The power conversion efficiency (PCE) of the PSCs significantly improved from 14.22% to 18.16% upon doping 2.0 wt % CuSCN with simultaneously enhanced open-circuit voltage, short-circuit current density, and fill factor. The long-term stability of the PSCs was also improved with significantly reduced PCE degradation (from 79% to 25%) after 200 h. Our results provide a simple method to improve the performance of planar PSCs by adding dopants into PTAA.

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Reference：
Copper catalysis in organic synthesis – NCBI,
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

Modeling chemical reactions helps engineers virtually understand the chemistry, optimal size and design of the system, and how it interacts with other physics that may come into play. Formula: CCuNS. Introducing a new discovery about 1111-67-7, Name is Cuprous thiocyanate

Single crystal X-ray structural characterizations are recorded for a wide range of adducts of the form MX:dppx (1:1)(n), M = silver(I) (predominantly), copper(I), X = simple (pseudo-) halide or oxy-anion (the latter spanning, where accessible, perchlorate, nitrate, carboxylate – a range of increasing basicity), dppx=bis(diphenylphosphino)alkane, Ph2P(CH 2)xPPh2, x = 3-6. Adducts are defined of two binuclear forms: (i) [LM(mu-X)2L], with each ligand chelating a single metal atom, and (ii) [M(mu-X)2(mu-(P-L-P?)) 2M?] where both ligands L and halides bridge the two metal atoms; a few adducts are defined as polymers, the ligands connecting M(mu-X)2M? kernels, this motif persisting in all forms. Synthetic procedures for all adducts have been reported. All compounds have been characterized both in solution (1H, 13C, 31P NMR, ESI MS) and in the solid state (IR).

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Formula: CCuNS. In my other articles, you can also check out more blogs about 1111-67-7

Reference：
Copper catalysis in organic synthesis – NCBI,
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

Researchers are common within chemical engineering and are often tasked with creating and developing new chemical techniques, frequently combining other advanced and emerging scientific areas. SDS of cas: 1111-67-7In an article, authors is Lobana, Tarlok S., once mentioned the new application about SDS of cas: 1111-67-7.

The reaction of copper(I) iodide with 1, 3-imidazolidine-2-thione (SC 3H6N2) in a 1:2 molar ratio (M/L) has formed unusual 1D polymers, {Cu6(mu3-SC3H 6N2)4(mu-SC3H6N 2)2(mu-I)2I4}n (1) and {Cu6(mu3-SC3H6N2) 2(mu-SC3H6N2)4(mu-I) 4I2}n (1a). A similar reaction with copper(I) bromide has formed a polymer {Cu6(mu3-SC 3H6N2)2(mu-SC3H 6N2)4(mu-Br)4Br2} n (3a), similar to 1a, along with a dimer, {Cu2(mu- SC3H6N2)2(eta1-SC 3H6N2)2Br2} (3). Copper(I) chloride behaved differently, and only an unsymmetrical dimer, {Cu2(mu-SC3H6N2) (eta1-SC3H6N2)3Cl 2} (4), was formed. Finally, reactions of copper-(I) thiocyanate in 1:1 or 1:2 molar ratios yielded a 3D polymer, {Cu2(mu-SC 3H6N2)2(mu-SCN)2} n (2). Crystal data: 1, C9H18Cu 3I3N6S3, triclinic, P1, a = 9.6646(11) A, b = 10.5520(13) A, c = 12.6177(15) A, alpha = 107.239(2), beta = 99.844(2), gamma = 113.682(2), V = 1061.8(2) A3, Z = 2, R = 0.0333; 2, C4H 6CuN3S2, monoclinic, P21/c, a = 7.864(3) A, b = 14.328(6) A, c = 6.737(2) A, beta = 100.07(3), V = 747.4(5), Z = 4, R = 0.0363; 3, C12H 24Br2Cu2N8S4, monoclinic, C2/c, a = 19.420(7) A, b = 7.686(3) A, c = 16.706(6) A, beta = 115.844(6), V = 2244.1(14) A3, Z = 4, R = 0.0228; 4, C12H24Cl2Cu2N8S 4, monoclinic, P21/c, a = 7,4500(6) A, b = 18.4965(15) A, c = 16.2131(14) A, beta = 95.036(2), V = 2225.5(3) A3, Z = 4, R = 0.0392. The 3D polymer 2 exhibits 20-membered metallacyclic rings in its structure, while synthesis of linear polymers; 1 and 1a, represents an unusual example of I (1a)-S (1) bond isomerism.

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Reference：
Copper catalysis in organic synthesis – NCBI,
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

Chemical engineers ensure the efficiency and safety of chemical processes, adapt the chemical make-up of products to meet environmental or economic needs, and apply new technologies to improve existing processes. Recommanded Product: Cuprous thiocyanate. Introducing a new discovery about 1111-67-7, Name is Cuprous thiocyanate

Equimolar reaction of copper(I) bromide with 2-thiouracil (tucH2) in acetonitrile-methanol formed a light yellow solid which on subsequent treatment with a mole of triphenyl phosphine (PPh3) in chloroform has yielded a sulfur-bridged dinuclear complex, [Cu2Br2(mu-S-tucH2)2(PPh3)2] 2CHCl3 1. A reaction of copper(I) bromide with two moles of 2,4-dithiouracil (dtucH2) in acetonitrile-methanol followed by addition of two moles of PPh3, designed to form [Cu(mu-S,S-dtuc)2(PPh3)4Cu] 2a, instead resulted in the formation of previously reported polymer, {CuBr(mu-S,S-dtucH2)(PPh3)}n 2. Reaction of copper(I) iodide with 2-thiouracil (tucH2) and PPh3 in 1:1:2 molar ratio (Cu:H2tuc:PPh3) as well as that of copper(I) thiocyanate with pyridine-2-thione (pySH) or pyrimidine-2-thione (pymSH) and PPh3 in similar ratio, yielded an iodo-bridged unsymmetrical dimer, [(PPh3)2(mu-I)2Cu(PPh3)] 3 and thiocyanate bridged symmetrical dimer, [(PPh3)2Cu(mu-N,S- SCN)2Cu(PPh3)2] 4, respectively. In both the latter reactions, thio-ligands which initially bind to Cu metal center, are de-ligated by PPh3 ligand. Crystal data: 1, P21/c: 173(2) K, monoclinic, a, 13.4900(6); b, 17.1639(5); c, 12.1860(5) A; beta, 111.807(5) a; R, 5.10%; 2, Pbca: 296(2) K, orthorhombic, a, 10.859(3); b, 17.718(4); c, 23.713(6) A; alpha=beta=gamma, 90 a; R, 4.60%; 3, P21: 173(2) K, monoclinic, a, 10.4208(7); b, 20.6402(12); c, 11.7260(7) A; beta, 105.601(7)a; R, 3.97%; 4, P-1: 173(2) K, triclinic, a, 10.2035(4); b, 13.0192(5); c, 13.3586(6) A; alpha, 114.856(4); beta, 92.872(4)a; gamma, 100.720(4)a; R, 3.71%. ESI-mass studies reveal different fragments of complexes.

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Reference：
Copper catalysis in organic synthesis – NCBI,
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”