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Six [Tp*WS3Cu2]-based clusters derived from [Et4N][Tp*WS3], Cu(i) salts and phosphine ligands: Syntheses, structures and enhanced third-order NLO properties

Treatment of [Et4N][Tp*WS3] (Tp* = hydridotris(3,5-dimethylpyrazol-1-yl)borate) (1) with CuX (X = Br, SCN) and PPh3 or 1,1-bis(diphenylphosphino)methane (dppm) produced two neutral trinuclear clusters [Tp*W(mu3-S)(mu-S)2Cu 2Br(PPh3)] (2) and [Tp*W(mu3-S)(mu-S) 2Cu2(SCN)(dppm)]2·MeCN·Et 2O (3·MeCN·Et2O). Reactions of 1 with [Cu(MeCN)4]PF6, NH4PF6 and 1,3-bis(diphenylphosphino)propane (dppp), N,N-bi(diphenylphosphanylmethyl)-2- aminopyridine (bdppmapy), N,N,N?,N?-tetra(diphenylphosphanylmethyl) ethylenediamine (dppeda), or 1,4-N,N,N?,N?- tetra(diphenylphosphanylmethyl)benzenediamine (dpppda) afforded four clusters containing butterfly-shaped [Tp*WS3Cu2] cores, [Tp*W(mu3-S)(mu-S)2Cu2(dpppds)] (PF6)·1.25MeCN (dpppds = 1,3-bis(diphenylphosphino)propane disulfide) (4·1.25MeCN), [Tp*W(mu3-S)(mu-S) 2Cu2(bdppmapy)](PF6)·3MeCN (5·3MeCN) and {[Tp*W(mu3-S)(mu-S)2Cu 2]2(L)]}(PF6)2·Sol (6·Et2O: L = dppeda, Sol = Et2O; 7·1.25MeCN: L = dpppda, Sol = 1.25MeCN). Compounds 2-7 were characterized by elemental analysis, IR, UV-Vis, 1H and 31P{1H} NMR spectra, electrospray ion mass spectra (ESI-MS) and single-crystal X-ray diffraction. Compound 2 or 3 has a butterfly-shaped [Tp*WS 3Cu2] core in which one [Tp*WS3] unit binds two Cu(i) centers via one mu3-S and two mu-S atoms. In the cationic structure of 4 or 5, one in situ-formed dpppds or bdppmapy combines with the [Tp*WS3Cu2] core via each of its two S atoms or two P atoms coordinated at each Cu(i) center. In the bicationic structure of 6 or 7, two [Tp*WS3Cu2] cores are linked by one dppeda or dpppda bridge to form a bicyclic structure. The isolation of 2-7 with unstable [Tp*WS3Cu2] cores may be ascribed to the coordination of P- or S-donor ligands at Cu(i) centers of these cores. The third-order nonlinear optical (NLO) properties of 2-7 in DMF were also investigated by using the femtosecond degenerate four-wave mixing (DFWM) technique at 800 nm.

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

 

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Reactions of a tungsten trisulfido complex of hydridotris(3,5- dimethylpyrazol-1-yl)borate (Tp*) [Et4N][Tp*WS 3] with CuX (X = Cl, NCS, or CN): Isolation, structures, and third-order NLO properties

Reactions of a tungsten trisulfido complex of hydridotris(3,5- dimethylpyrazol-1-yl)borate (Tp*) [Et4N][Tp*WS 3] (1) with 3 equiv of CuCl in CHCl3 afforded a tetranuclear anionic cluster [Et4N][Tp*W(mu3-S) 3(CuCl)3] (2), while that of 1 with 3 equiv of CuNCS in MeCN produced a decanuclear neutral cluster (major product) [Tp*W(mu3-S)3Cu3(mu-NCS) 3(CuMeCN)]2 (3) along with a binuclear anionic cluster (minor product) [Et4N][Tp*WO(mu-S)2(CuNCS)] (4). Solvothermal reactions of 1 with 3 equiv of CuCN in MeCN at 80C for 48 h followed by slowly cooling it to ambient temperature gave rise to a polymeric cluster [Tp*W(mu3-S)(mu-S)2Cu 2(MeCN)(mu-CN)]n (5). Compounds 2-5 were characterized by elemental analysis, IR, UV-vis, 1H NMR, and single-crystal X-ray crystallography. The cluster anion of 2 has a [Tp*WS3Cu 3] incomplete cube with one Cl atom coordinated at each Cu center. 3 is composed of an unprecedented centrosymmetric W2Cu8 cluster core in which each void of the two single incomplete cubane-like [Tp*W(mu3-S)3Cu3(mu-NCS)] + cations is partially filled with an extra [Cu(MeCN)(mu-NCS) 2]- anion via a pair of Cu-mu-NCS-Cu bridges. The cluster anion of 4 contains one WS2Cu core that is formed by an oxidized [Tp*WO-(mu-S)2] species and one CuNCS fragment. 5 consists of butterfly shaped [Tp*W(mu3-S)(mu-S) 2Cu2(MeCN)] fragments that are interconnected via cyanide bridges to form a 1D spiral chain extending along the c axis. The successful synthesis of 2-5 from 1 suggests that 1 may be an excellent synthon to the W/Cu/S clusters. In addition, the third-order nonlinear optical (NLO) properties of 1-3 in solution were also investigated by femtosecond degenerate four-wave mixing (DFWM) technique with a 80 fs pulse width at 800 nm. Although 2 was not detected to have NLO effects, 1 and 3 exhibited relatively good optical nonlinearities with the nonlinear refractive index n2 and the third-order nonlinear optical susceptibility chi(3) values being 0.79 × 10-13 and 0.38 × 10-14 esu (1) and 2.08 × 10-13 and 1.00 × 10-14 esu (3), respectively. The second-order hyperpolarizability gamma value for 3 (5.46 × 10-32 esu) is ca. 5 times larger than that of its precursor 1.

The proportionality constant is the rate constant for the particular unimolecular reaction. the reaction rate is directly proportional to the concentration of the reactant. I hope my blog about 1111-67-7 is helpful to your research. Safety of Cuprous thiocyanate

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

 

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The proportionality constant is the rate constant for the particular unimolecular reaction. the reaction rate is directly proportional to the concentration of the reactant. I hope my blog about 1111-67-7 is helpful to your research. name: Cuprous thiocyanate

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Phase evolution of Cu-S system in ethylene glycol solution: The effect of anion and PVP on the transformation of thiourea

The transformation mechanisms of thiourea in ethylene glycol solution was systematically investigated in this report, which shows the transformation process is influenced by the anion (NO3-, Cl-, Br -) and polyvinylpyrrolidone (PVP). Thiourea (tu) isomerizes into ammonium thiocyanate when NO3- is present, regardless of the existence of PVP. For Cl-, thiourea coordinates with copper anion to form [Cu(tu)]Cl·1/2H2O complex whether PVP is present. When it comes to Br-, thiourea hydrolyzes in the cooperation of PVP or coordinates with copper anion to form [Cu(tu)Br]·1/2H2O complex without PVP. The different transformation routes will lead to different phase evolution of the Cu-S system. This work may provide a new understanding of the transformation of thiourea in ethylene glycol solution. The optical properties of the as-prepared copper sulfides exhibit signi?cant stoichiometry-dependent features which may have potential applications in semiconductor photovoltaic devices. The effect of anions and PVP on the transition of thiourea in ethylene glycol solution was studied in detail. Copyright

The proportionality constant is the rate constant for the particular unimolecular reaction. the reaction rate is directly proportional to the concentration of the reactant. I hope my blog about 1111-67-7 is helpful to your research. name: Cuprous thiocyanate

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

 

The important role of Cuprous thiocyanate

Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data. Safety of Cuprous thiocyanate, If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 1111-67-7, in my other articles.

Because a catalyst decreases the height of the energy barrier, Safety of Cuprous thiocyanate, its presence increases the reaction rates of both the forward and the reverse reactions by the same amount.Safety of Cuprous thiocyanate, Name is Cuprous thiocyanate, molecular formula is CCuNS. In a article,once mentioned of Safety of Cuprous thiocyanate

[BF4]: A useful synthon for multiple cage boron functionalizations of o -carborane

A simple and efficient method for selective cage B(3) multiple functionalization of o-carborane is described. Reaction of [3-N2-o-C2B10H11][BF4] with various kinds of nucleophiles gave a very broad spectrum of cage B(3)-substituted o-carborane derivatives, 3-X-o-C2B10H11 (X = OH, SCN, NH2, NO2, N3, CF3, PO(C6H5)2, etc). This reaction may serve as another efficient [18F]-radiolabeling method of carborane clusters for positron emission tomography applications.

Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data. Safety of Cuprous thiocyanate, If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 1111-67-7, in my other articles.

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

 

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A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, HPLC of Formula: CCuNS, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. HPLC of Formula: CCuNS, Name is Cuprous thiocyanate, molecular formula is CCuNS. In a Article, authors is Zheng, He-Gen,once mentioned of HPLC of Formula: CCuNS

Syntheses, crystal structures and nonlinear optical properties of heteronuclear clusters [MS4Cu4(SCN)2(NC5H5) 6] (M=W, Mo)

The title compounds [MS4Cu4(SCN)2(NC5H5) 6] (M=W (1); M=Mo (2); NC5H5=pyridine) were obtained by the reaction of (NH4)2MS4, CuSCN, KSCN and pyridine. The X-ray analyses of 1 and 2 show that four edges of the tetrahedral MS42- core are coordinated by four copper atoms, giving an MS4Cu4 aggregate of approximate D2h symmetry. The nonlinear optical properties of 1 and 2 were investigated by a Z-scan technique with 7 ns laser pulses of 532 nm. The third-order nonlinearities were determined with alpha2=4.3×10-5 and 4.1×10-5 cm W-1 M-1; and n2=-4.3×10-10 and -4.1×10-10 cm2 W-1 M-1, respectively, for compounds 1 and 2.

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

 

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Synthesis and crystal structure of Me3NHCu2(SCN)3, Me2C=NMe2Cu2(SCN)3, and Me2C=NMe2Ag2(SCN)3. Three-dimensional networks of thiocyanatometallates(I)

Attempts to build up polyanionic networks on the basis of thiocyanatometallates of Cu1 and Ag1 led to the synthesis of three new tris(thiocyanato)dimetallates(I) A[M2(SCN)3] with M = Cu, Ag and A = Me3NH and A = [Me2CNMe2]. The crystal structures show distorted tetrahedral [M(SCN)3(NCS)] and [M(SCN)2(NCS)2] building groups interlinked by SCN bridges. The resulting 3-dimensional frame works accommodate the counter cations in spacious voids. Me3NHCu2(SCN)3 (1) was synthesized by reaction of CuSCN with (CH3)3NHCl in the presence of an excess of KSCN in acetone. 1 crystallizes in the monoclinic space group P21/c with a = 578.4(1), b = 3025.1(5), c = 754.7(3) pm; beta = 112.53; Z = 4. The reaction of CuSCN or AgSCN with (CH3)2NH2Cl and KSCN in acetone resulted in the formation of [Me2CNMe2]Cu2(SCN)3 (2) and [Me2CN-Me2]Ag2(SCN)3 (3). Compound 2 crystallizes in the orthorhombic space group P212121 with a = 720.6(1), b= 1161.5(1), c = 1655.0(2) pm; Z = 4. The isotypical structure of 3 exhibits somewhat larger unit cell dimensions; a = 743.4(1), b = 1222.5(1), c = 1683.9(2) pm.

Interested yet? Keep reading other articles of Reference of 62348-13-4!, Application In Synthesis of Cuprous thiocyanate

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

 

Extracurricular laboratory:new discovery of Cuprous thiocyanate

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Organocuprate cross-coupling: The central role of the copper(III) intermediate and the importance of the copper(I) precursor

(Chemical Equation Presented) CuIII in focus: The key intermediate in copper-mediated cross-coupling reactions has long been believed to be a “copper-(III) intermediate”. Investigation of reactions of a variety of methyl Gilman reagents Me2CuLi·LiX with Etl using rapid-injection NMR spectroscopy conditions reveals a number of formally Cu III tetra-coordinate square-planar intermediates (see scheme) with a surprising range of stabilities.

Do you like my blog? If you like, you can also browse other articles about this kind. Thanks for taking the time to read the blog about 1111-67-7

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

 

Extracurricular laboratory:new discovery of 1111-67-7

Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data. Safety of Cuprous thiocyanate, If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 1111-67-7, in my other articles.

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Di(2-pyridyl) ketone complexes of CuI- and Cu II-containing iodide and thiocyanate ligands: An unusual case of a mixed-aldol condensation

Complexes containing di(2-pyridyl) ketone (dpk) as a bi- (N,N) and tridentate (N,N,O) ligand have been synthesised1,2 and characterized by spectral and structural studies. Products 1 and 2 are polymorphs of the polymeric copper(I) complex [Cu(dpk)(NCS)]n containing dpk with thiocyanate anions which bridge to form a one-dimensional continuous polymer chain. The novel dinuclear copper(II) complex [Cu2(dpkA·acetone) 2(NCS)2] (3) was formed when 1 and 2 were allowed to stand in the supernatant. In this instance it appears that a transition-metal- promoted aldol condensation has occurred between the solvent acetone and the ketone carbonyl of dpk to produce the novel ligand, dpkA·acetone. Product 3 contains two five-coordinate copper(II) ions, both with trigonal bipyramidal coordination, bridged through deprotonated hydroxy groups on each dpkA·acetone. A chemical rationalisation for the formation of 3 is proposed. The dinuclear copper(I) complex [Cu2(dpk)2I 2] (4) is also reported, which contains two four-coordinate copper(I) ions that are bridged together through iodide ions.

Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data. Safety of Cuprous thiocyanate, If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 1111-67-7, in my other articles.

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

 

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Two type skeleton heterobimetallic trinuclear Cu-Mo-S clusters containing closo carborane diphosphine ligand 1,2-bis(diphenylphosphino)-1,2-dicarba-closo-dodecaborane

The carborane skeleton was introduced into the heterometallic sulfide cluster cores. Two heterobimetallic trinuclear Cu-Mo-S clusters with linear or butterfly-shaped skeleton containing 1,2-bis(diphenylphosphino)-1,2-dicarba-closo-dodecaborane have been synthesized by the reactions of (NH4)2MoS4 or (NH4)2MoOS3, CuSCN with 1,2-(PPh2)2-1,2-C2B10H10 (L) in dichloromethane and characterized by elemental analysis, FT-IR, UV/Visible, 1H and 13C NMR spectroscopy and X-ray structure determination.

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

 

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Carbon Nano-Onions as a Functional Dopant to Modify Hole Transporting Layers for Improving Stability and Performance of Planar Perovskite Solar Cells

Poly (3,4-ethylenedioxythiophene) polystyrene sulphonate (PEDOT:PSS) is the most widely used hole transporting layer (HTL) in planar perovskite solar cells, which shows excellent optical, electrical properties and good compatibility with low temperature, solution and flexible processing. Nevertheless, the acidic and hygroscopic property of PEDOT:PSS restricts its film conductivity and leads to the degradation of device stability. Herein, for the first time, we introduce the unprecedentedly zero-dimensional dopant of carbon nano-onions (CNOs) and the functionalized oxidized carbon nano-onions (ox-CNOs) to modify the PEDOT:PSS HTL. Besides the merits of high conductivity and suitable energy level, the CNOs and ox-CNOs modified PEDOT:PSS HTLs could provide a superior perovskite crystalline film with large-scale grains and orderly grain boundaries exhibiting a high surface tension with the hydrophobic property, resulting in a significant enhancement of PCE from 11.07% to 15.26%. Moreover, by suppressing the corrosion effect of PEDOT:PSS on ITO electrode, a dramatic improvement in the device stability has also been obtained.

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