Day: October 21, 2020

Dichlorotris(triphenylphosphino)ruthenium (II), cas is 15529-49-4, it is a common heterocyclic compound, the ruthenium-catalysts compound, its synthesis route is as follows.,15529-49-4

A 50 ml three-necked flask equipped with a stirring reflux device was charged with 1 mmol of 2-diphenylphosphineaniline,2 mmol of benzyl alcohol, 1 mmol of bisdiphenylphosphinemethane, 1 mmol of RuCl2 (PPh3) 3,2 mmol of triethylamine, 20 ml of toluene, heating at 110 C. for 12 h under a nitrogen atmosphere, cooling,The resulting solid was recrystallized from a mixed solvent of CH 2 Cl 2 and petroleum ether to give product 1 in a yield of 89%.

With the rapid development of chemical substances, we look forward to future research findings about Dichlorotris(triphenylphosphino)ruthenium (II)

Reference£º
Patent; Luoyang Normal College; Li Hongmei; Xu Chen; Zu Enpu; Xiao Zhiqiang; Han Xin; (12 pag.)CN104804048; (2017); B;,
Highly efficient and robust molecular ruthenium catalysts for water oxidation
Catalysts | Special Issue : Ruthenium Catalysts – MDPI

As a common heterocyclic compound, it belongs to quinuclidine compound,Quinuclidine-4-carboxylic acid hydrochloride,40117-63-3,Molecular formula: C8H14ClNO280,mainly used in chemical industry, its synthesis route is as follows.,246047-72-3

Grubbs second generation catalyst (100 mg, 0.117 mmol), 2-[(2,6-dimethylphenylimino)methyl]phenol (pKa: 8.85+/- 0.30) (0.117 mmol), silver (I) carbonate (16.27 mg, 0.058 mmol), and THF (2 ml) were reacted at room temperature during 2 h. The solvent was evaporated and crude reaction product purified on a chromatography column to give an orange-brown complex. Yield 22%.

With the synthetic route has been constantly updated, we look forward to future research findings about (1,3-Bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene)dichloro(phenylmethylene)(tricyclohexylphosphine)ruthenium,belong ruthenium-catalysts compound

Reference£º
Patent; Telene SAS; EP2151445; (2010); A1;,
Highly efficient and robust molecular ruthenium catalysts for water oxidation
Catalysts | Special Issue : Ruthenium Catalysts – MDPI

15529-49-4, Dichlorotris(triphenylphosphino)ruthenium (II) is a ruthenium-catalysts compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated

An anhydrous Et2NH (10 mL) solution of dicyclohexylphosphinomethylpyridine-borane complex (280 mg, 0.923 mmol) was heated at 65C for 48 h under Ar. The solution was cooled to room temperature and Et2NH was removed in vacuo (ca. 10 mmHg, room temperature). To the residue was added sequentially dichlorotris(triphenylphosphino)ruthenium (II) (442.5 mg, 0.46 mmol) and an anhydrous toluene (10 mL). The resulting mixture was heated at 110C for 5 h under Ar, and was cooled to room temperature. Then to the mixture was added an anhydrous hexane (20 mL) to afford the yellow suspension. The mixture of the suspension was stirred at room temperature for 12 h and filtered through a filtration paper. The obtained yellowish orange solid was dried in vacuo (ca. 0.1 mmHg, room temperature) and dissolved in CH2Cl2. This solution was purified by column chromatography on silica gel (EtOAc/hexane =1/4) to afford RUPCY (1a) as orange powder (237 mg, 68%)., 15529-49-4

The synthetic route of 15529-49-4 has been constantly updated, and we look forward to future research findings.

Reference£º
Article; Miura, Takashi; Held, Ingmar E.; Oishi, Shunsuke; Naruto, Masayuki; Saito, Susumu; Tetrahedron Letters; vol. 54; 21; (2013); p. 2674 – 2678;,
Highly efficient and robust molecular ruthenium catalysts for water oxidation
Catalysts | Special Issue : Ruthenium Catalysts – MDPI

Name is Dichlorotris(triphenylphosphino)ruthenium (II), as a common heterocyclic compound, it belongs to ruthenium-catalysts compound, and cas is 15529-49-4, its synthesis route is as follows.,15529-49-4

The complex RuCl2(PPh3)3 (4) (0.150 g, 0.156 mmol) suspended in 2 ml of distilled toluene, was reacted with HCNN-H (1) (36 mg, 0.174 mmol) and triethylamine (0.22 ml, 0.158 mmol). After stirring the mixture for 2 hours at 110 ?C the solution volume was reduced to about half and the complex was precipitated by adding 2 ml of pentane. The solid obtained was filtered off, washed with pentane (3 x 5 ml) and dried under reduced pressure. Yield 100 mg (74%). Elemental analysis (%) calculated for C50H41ClN2P2Ru. C, 69.16; H, 4.76; N, 3.23. Found: C, 69.35; H, 4.85; N, 3.34. 31P{1H} NMR (81.0 MHz, CD2Cl2, 20 C, H3PO4): delta 56.5 (d, J(PP) = 33.4 Hz), 50.5 (d, J(PP)= 33.4 Hz).

With the complex challenges of chemical substances, we look forward to future research findings about Dichlorotris(triphenylphosphino)ruthenium (II)

Reference£º
Patent; Universita’ Degli Studi di Udine; RIGO, Pierluigi; BARATTA, Walter; SIEGA, Katia; CHELUCCI, Giorgio Adolfo; BALLICO, Maurizio; MAGNOLIA, Santo; EP2178843; (2013); B1;,
Highly efficient and robust molecular ruthenium catalysts for water oxidation
Catalysts | Special Issue : Ruthenium Catalysts – MDPI

(1,3-Bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene)dichloro(phenylmethylene)(tricyclohexylphosphine)ruthenium, cas is 246047-72-3, it is a common heterocyclic compound, the ruthenium-catalysts compound, its synthesis route is as follows.,246047-72-3

After a 50 mL two-necked flask was purged with argon, the ligand 7t (10 mmol), 30 mL of CuCl (30 mmol, 3 eq) and 30 mL of dry DCM were sequentially added and the mixture was purged three times with argon to protect the closed system with argon balloon. Ruthenium complex 1b (12 mmol) was added under argon atmosphere, and the reaction was carried out at room temperature for 0.5 hour. After the reaction was over, silica gel was added to the filtrate to produce sand after filtration. The crude product was obtained by silica gel column chromatography, and then washed with methanol or pentane-DCM to obtain 8t as a green solid product in a yield of 87%.

With the rapid development of chemical substances, we look forward to future research findings about (1,3-Bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene)dichloro(phenylmethylene)(tricyclohexylphosphine)ruthenium

Reference£º
Patent; Zannan Science And Technology (Shanghai) Co., Ltd.; Zhan Zhengyun; (102 pag.)CN104262403; (2017); B;,
Highly efficient and robust molecular ruthenium catalysts for water oxidation
Catalysts | Special Issue : Ruthenium Catalysts – MDPI

As a common heterocyclic compound, it belongs to ruthenium-catalysts compound, name is Dichlorotris(triphenylphosphino)ruthenium (II), and cas is 15529-49-4, its synthesis route is as follows.,15529-49-4

To a solution of N,O-LH-Cl (930?mg, 4.0?mmol) in THF (20?mL) was added [Ru(PPh3)3Cl2] (868?mg, 2.0?mmol), which was then stirred under N2 for 15?min. Triethylamine (Et3N) (404?mg, 4.0?mmol) was introduced, and the reaction mixture was stirred overnight at room temperature, during which the color of solution changed from brown to dark green. After removal of solvents in vacuo, the residue was extracted with CH2Cl2 (5?mL?*?2) and the solution was filtered. The filtrate was layered with Et2O (20?mL) at room temperature, and dark green block-shaped crystals of cis-[RuCl(PPh3)(kappa2-N,O-L-Cl)2] (1) were harvested in three days. Yield: 1187?mg, 69% (based on Ru). mueff?=?1.98?muB. IR (KBr disc, cm-1): 1592 (nuC=N), 1314 (nuC-O), 1437, 1092 and 698 (nuPPh3). MS (FAB): m/z 860 [M+], 825 [M+-Cl], 598 [M+-PPh3], 563 [Ru(kappa2-N,O-L-Cl)2]+. Anal. Calc. for C44H33N2O2Cl3PRu(%): C, 61.44; H, 3.87; N, 3.26. Found: C, 61.47; H, 3.83; N, 3.24.

With the complex challenges of chemical substances, we look forward to future research findings about 15529-49-4,belong ruthenium-catalysts compound

Reference£º
Article; Tang, Li-Hua; Wu, Fule; Lin, Hui; Jia, Ai-Quan; Zhang, Qian-Feng; Inorganica Chimica Acta; vol. 477; (2018); p. 212 – 218;,
Highly efficient and robust molecular ruthenium catalysts for water oxidation
Catalysts | Special Issue : Ruthenium Catalysts – MDPI

As a common heterocyclic compound, it belongs to ruthenium-catalysts compound, name is (1,3-Bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene)dichloro(phenylmethylene)(tricyclohexylphosphine)ruthenium, and cas is 246047-72-3, its synthesis route is as follows.,246047-72-3

Example 3 – Synthesis of the complex 3 according to the invention The commercially available complex G (200 mg, 0.24 mmol) was placed in a flask, to which methylene chloride was added (6 ml). This was followed by adding the compound of the formula: (63 mg, 0.47 mmol) and tricyclohexylphosphine (132 mg, 0.47 mmol). The resulting solution was stirred at a temperature of 40C for 5 hours. The reaction mixture was introduced at the top of a chromatographic column packed with silica gel (eluent: ethyl acetate/cyclohexane, 0 to 10 vol.%). After evaporating the solvents, the complex 3 was obtained as a green solid (140 mg, 72% yield). 3 H NMR (500 MHz, CD2Cl2) delta ppm: 15.85 (s, 1H), 7.07 (s, 1H), 7.00-6.96 (m, 3H), 6.66 (d, J = 8.4 Hz, 1H), 6.44 (dd, J = 7.7, 1.4 Hz, 1H), 6.24 (s, 1H), 6.20 (t, J = 7.2 Hz, 1H), 4.01-3.96 (m, 1H), 3.83-3.70 (m, 2H), 3.64-3.59 (m, 1H), 2.63 (s, 3H), 2.54 (s, 3H), 2.50 (s, 3H), 2.35 (s, 3H), 2.27 (s, 3H), 1.66-1.50 (m, 13H), 1.29 (s, 3H), 1.11-0.70 (m, 20H). 13C NMR: (125 MHz, CD2CI2) delta ppm: 281.36, 222.21, 221.66, 180.31, 148.30, 139.54, 139.17, 138.78, 137.63, 137.32, 136.98, 134.69, 130.23, 130.05, 129.70, 129.00, 122.38, 116.17, 111.26, 32.52, 32.39, 29.45, 28.92, 28.23, 28.15, 28.12, 28.04, 27.34, 27.03, 21.33, 21.14, 19.40, 18.92, 18.66, 16.76. 31P NMR (124.5 MHz, CDCI3) delta ppm: 29.11.

With the complex challenges of chemical substances, we look forward to future research findings about (1,3-Bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene)dichloro(phenylmethylene)(tricyclohexylphosphine)ruthenium

Reference£º
Patent; APEIRON SYNTHESIS S.A.; SKOWERSKI, Krzysztof; BIENIEK, Micha?; WO2014/16422; (2014); A1;,
Highly efficient and robust molecular ruthenium catalysts for water oxidation
Catalysts | Special Issue : Ruthenium Catalysts – MDPI

Name is (1,3-Bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene)dichloro(phenylmethylene)(tricyclohexylphosphine)ruthenium, as a common heterocyclic compound, it belongs to ruthenium-catalysts compound, and cas is 246047-72-3, its synthesis route is as follows.,246047-72-3

To a solution of 18 (10.5 g, 22.4 mmol) in THF (120 mL) was added TBAF (1.0 mol/L in THF, 90 mL, 90 mmol) at 20 C, and the mixture was stirred for 5 h. Then, the mixture was concentrated under reduced pressure, and the residue was purified by recrystallization (PhH + H2O) to give 19 (7.50 g, 21.2 mmol, 95%) as a colorless needle. 19: mp 217e219 C; [a]D24 39.7 (c 0.0350, CHCl3); IR (KBr) n 3484, 3054, 3026, 2891, 1436, 1380, 1265, 1103, 1031, 861, 828, 801, 744, 678, 549, 476 cm1; 1H NMR (400 MHz, CDCl3) d 2.36e2.45 (1H, m), 2.66 (1H, ddd, J 3.6, 8.3, 15.9 Hz), 2.80 (1H, s), 3.34 (1H, t, J 8.5 Hz), 3.39 (1H, ddd, J 4.0, 9.7, 19.4 Hz), 3.53 (1H, dt, J 5.2, 9.7 Hz), 3.65 (1H, t, J 9.3 Hz), 3.77 (1H, t, J 10.5 Hz), 3.89 (1H, t, J 8.8 Hz), 4.07 (1H, brqd, J 2.9, 15.3 Hz), 4.35e4.40 (2H, m), 5.73(1H, s), 5.82e5.88 (1H, m), 5.92e5.98 (1H, m), 7.46e7.50 (2H, m), 7.62 (1H, d, J 8.5 Hz), 7.82e7.88 (3H, m), 7.99 (1H, s); 13C NMR (100 MHz, CDCl3) d 34.3 (CH2), 68.5 (CH2), 68.9 (CH2), 69.9 (CH), 73.6 (CH), 76.4 (CH), 80.9 (CH), 87.8 (CH), 101.9 (CH), 123.8 (CH), 125.8 (CH), 126.1 (CH), 126.4 (CH), 127.3 (CH), 127.7 (CH), 128.2 (CH),128.4 (CH), 131.7 (CH), 132.9 (C), 133.7 (C), 134.4 (C); EI-HRMS (m/z) calcd for C21H22O5 [M]: 354.1467, found: 354.1464.

With the complex challenges of chemical substances, we look forward to future research findings about (1,3-Bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene)dichloro(phenylmethylene)(tricyclohexylphosphine)ruthenium

Reference£º
Article; Sato, Takuto; Nogoshi, Keisuke; Goto, Akiyoshi; Domon, Daisuke; Kawamura, Natsumi; Nomura, Yoshitaka; Sato, Daisuke; Tanaka, Hideki; Murai, Akio; Katoono, Ryo; Kawai, Hidetoshi; Suzuki, Takanori; Fujiwara, Kenshu; Kondo, Yoshihiko; Akiba, Uichi; Tetrahedron; vol. 73; 6; (2017); p. 703 – 726;,
Highly efficient and robust molecular ruthenium catalysts for water oxidation
Catalysts | Special Issue : Ruthenium Catalysts – MDPI

Name is Dichlorotris(triphenylphosphino)ruthenium (II), as a common heterocyclic compound, it belongs to ruthenium-catalysts compound, and cas is 15529-49-4, its synthesis route is as follows.,15529-49-4

General procedure: The amine (4-CH3-pip, 4-CH2Ph-pip or 4-CH2(OH)-pip;0.34 mmol) was added to a solution of [RuCl2(PPh3)3] (0.26 mmol;0.25 g) in acetone (40 mL). The resulting dark green solution wasstirred for 2 h at RT. A green precipitate was formed, filtered,washed with methanol and ethyl ether, and then dried in vacuum.Complex 3 (R = OH): 67% yield. Analytical data for RuCl2P2NC42H43O are 62.15C, 5.34H, and 1.73% N; found 62.19C, 5.26H, and 1.83% N. FTIR in CsI: 323 for cm-1 for nu(Ru-Cl); 3230 cm-1 nu(N-H). 31P{1H} NMR in CDCl3: 62.7 ppm (s).

With the complex challenges of chemical substances, we look forward to future research findings about Dichlorotris(triphenylphosphino)ruthenium (II)

Reference£º
Article; Chaves, Henrique K.; Ferraz, Camila P.; Carvalho Jr., Valdemiro P.; Lima-Neto, Benedito S.; Journal of Molecular Catalysis A: Chemical; vol. 385; (2014); p. 46 – 53;,
Highly efficient and robust molecular ruthenium catalysts for water oxidation
Catalysts | Special Issue : Ruthenium Catalysts – MDPI

As a common heterocyclic compound, it belongs to ruthenium-catalysts compound, name is (1,3-Bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene)dichloro(phenylmethylene)(tricyclohexylphosphine)ruthenium, and cas is 246047-72-3, its synthesis route is as follows.,246047-72-3

A suspension of 1.00 g (1.18 mmol) of [RuCl2(PCy3)(ImH2Mes)(phenylmethylene)] (commercially available from Sigma- Aldrich Inc., St. Louis, USA), 0.13 g (1.30 mmol) of copper chloride and 0.36 g (1.30 mmol) of 2-[((?,Z)-2-propenyl)-phenoxy]-l -pyrrolidine- 1-yl- propan-1-one as a 4:1 mixture ofE/Z-isomers in 75 ml of dichloromethane was stirred for 30 min at 400C. The reaction mixture was evaporated to dryness at 400C/ 10 mbar. The residue was stirred in 60 ml of ethyl acetate for 30 min at room temperature. The dark green suspension was filtered and the filtrate was evaporated to dryness at 40C/10 mbar. The crude title product was purified by silica gel chromatography (dichloromethane/methanol 98:2) to yield 0.52 g (62% yield) of the title compound as a green powder.MS: 709.2 (M+). Anal, calcd. for C35H43Cl2N3O2Ru ? 0.85 CH2Cl2: C, 55.04; H, 5.76; N, 5.37, Cl 16.83. Found: C, 54.52; H, 5.74; N, 5.29, Cl 16.82.

With the complex challenges of chemical substances, we look forward to future research findings about 246047-72-3,belong ruthenium-catalysts compound

Reference£º
Patent; F. HOFFMANN-LA ROCHE AG; WO2009/124853; (2009); A1;,
Highly efficient and robust molecular ruthenium catalysts for water oxidation
Catalysts | Special Issue : Ruthenium Catalysts – MDPI