Category: ruthenium-catalysts

With the rapid development and complex challenges of chemical substances, new drug synthesis pathways are usually the most effective.15529-49-4,Dichlorotris(triphenylphosphino)ruthenium (II),as a common compound, the synthetic route is as follows.

Example B2: Preparation of [(CI)2Ru(Pphenyl3)(ligand L2)], K2tolueneyl 272.5 mg (0.284 mmol) of dichlorotris(triphenylphosphine)ruthenium(ll) and 160.0 mg (0.296 mmol) of ligand L2 are placed in a 10 ml Schlenk tube and admixed with 6.5 ml of dry toluene under argon. The dark suspension is stirred overnight at room temperature, resulting in a colour change to orange-red. After addition of 4 ml of dry pentane, the stirrer is switched off and the supernatant orange solution is filtered off with suction from the orange solid. The solid is washed five times with 4 ml each time of pentane and dried in a high vacuum. This gives 244 mg (88% of theory) of the title compound as an orange powder. 31P-NMR (C6D6, 121.5 MHz, ppm): 49.7 (d, J = 40), 61.2 (d, J = 40).

As the paragraph descriping shows that 15529-49-4 is playing an increasingly important role.

Reference£º
Patent; SOLVIAS AG; WO2007/104690; (2007); A1;,
Highly efficient and robust molecular ruthenium catalysts for water oxidation
Catalysts | Special Issue : Ruthenium Catalysts – MDPI

With the rapid development and complex challenges of chemical substances, new drug synthesis pathways are usually the most effective.15529-49-4,Dichlorotris(triphenylphosphino)ruthenium (II),as a common compound, the synthetic route is as follows.

RuCl2(PPh3)3(480 mg, 0.5 mmol) was placed in a 25 mL flask filled with argon. THF(12.5 mL) and (R,R)-DPEN (127 mg, 0.6 mmol) were then added. The mixturewas degassed and stirred under argon at 25 oC for 6 h. After removalof turbidity by filtration, n-hexane (30 mL) was added, and a light yellowsolid was obtained. The supernatant was removed and the resulting solid wasdried under reduced pressure to give analytically pure 1f (442 mg, 97% yield). 2.1. RuCl2(R,R)-DPEN(PPh3)2 1f1H NMR (300MHz, C6D6, ppm), delta: 7.95-7.92 (m,12H), 6.97-6.95 (m, 18H), 6.74 (br, 10H), 4.61-4.4.59(m, 2H), 4.12-4.09 (m, 2H), 3.59-3.56 (m, 2H); 31P NMR (121MHz, C6D6, ppm), delta: 45.7.

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

Reference£º
Article; Li, Xuefeng; Ma, Yaping; Xing, Zhikui; Tang, Ning; Zhu, Jin; Deng, Jingen; Tetrahedron Letters; vol. 55; 29; (2014); p. 3868 – 3872;,
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

A 50 ml three-necked flask equipped with a stirring reflux device was charged with 1 mmol of 2-dicyclohexylphosphine aniline,1.2 mmol of p-chlorobenzyl alcohol, 1 mmol of 1,1′-diphenylphosphinoferrocene, 1 mmol of RuCl2 (PPh3) 3, 1.2 mmol of triethylamine and 20 ml of toluene at a temperature of 110 C. and heated under a nitrogen atmosphere for 24 hAfter cooling and filtration, the resulting solid was recrystallized from a mixed solvent of CH 2 Cl 2 and petroleum ether to give product 20 in a yield of 86%.

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

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

With the rapid development and complex challenges of chemical substances, new drug synthesis pathways are usually the most effective.15529-49-4,Dichlorotris(triphenylphosphino)ruthenium (II),as a common compound, the synthetic route is as follows.

cis-cis- 1,3,5-triaminocyclohexane (30.0 nig, 0.232 mmol) was added to an ampoule charged with dichlorotris(triphenylphosphane)ruthenium(II) (196 mg, 0.204 mmol) dissolved in dichloromethane (20 mL), causing an instant colour change from black to orange. The solution was stirred at 50C for 4 days in the sealed vessel, during whichtime the solution changed colour to yellow and a white precipitate formed. The precipitate was removed by filtration and the filtrate reduced in volume to approx. 1 mL in vacuo. The product was precipitated by addition of pentane (20 mL) as an orange powder, and washed twice with pentane (20 mL). Yield: 115 mg (86.8 %, 0.177 mmol of RuCl2(K3-c -tach)(PPh3).CH2Cl2). NMR Spectroscopy Cs minor plane H NMR (CD2C12, 399.8 MHz, 293K) delta 7.85 (app t, HH = 7.5 Hz, VHP = 5.8 Hz, VHH = 1.5 Hz, 6H, P/Vz3, Ar2), 7.36 (m, 9H, Rho/>Lambda3, Ar3 + Ar4), 4.77 (s, 2H, NH2, N1), 3.90 (bs, 1Eta, CH, Cy1), 2.92 (s, 2Eta, CH, Cy2), 2.65 (d, VHH = 10.6 Hz, 2H, N N2), 1.92 (s, 4H, CH2, Cy3), 1.85 (d, HH = 10.6 Hz, 2H, NH2, N2), 1.62 (d, VHH = 15.3 Hz, 1H, CH2, Cy4), 1.00 (d, VHH = 15.3 Hz, 1H, CH2, Cy4); 31Rho{} NMR (CD2C12, 161.8 MHz, 293 ) delta 66.0 (s, IP, PPh3); “Ci’H} NMR (CD2C12, 100.5 MHz, 293K) delta 136.2 (d, ‘Jpc = 36.0 Hz, VPh3, Ar1), 134.2 (d, VPC = 10.1 Hz, VPh3, Ar2), 129.5 (d, VPC = 1.85 Hz, ?P 3, Ar4), 128.8 (d, VPC = 8.7 Hz, ?Ph3, Ar3), 44.0 (s, CH, Cy1), 43.8 (s, CH, Cy2), 35.0 (s, CH2, Cy3), 33.6 (s, CH2, Cy4).Mass Spectrometry ESI-MS: m/z 569.1186 ([RuCl(NCMe)( 3-c i-tach)(PPh3)l+. Calc 569.1173, 100 %), 528.0919 ([RuCl(K3-c-tach)(PPh3)]+; 528.0907, 25), 246.5607 ([RU(K3-CW- tach)(PPh3)]2+, 246.5608, 10). Infra-Red Spectroscopy ATR-IR: (cm 1) 3462, 3283, 3240, 3050, 2888, 1649, 1588, 1480, 1432 (P-Ph), 1367, 1346, 1270, 1211, 1183, 1156, 1089, 1027, 968, 905. Elemental Analysis CH2C12 c / % H / % N / % Found 46.25 4.92 6.43 0 51.15 5.37 7.46 1 46.31 4.97 6.48 Table 0.1: CHN Elemental analysis for RuCl2(K3-cw-tach)(PPh3)

As the paragraph descriping shows that 15529-49-4 is playing an increasingly important role.

Reference£º
Patent; UNIVERSITY OF YORK; GAMBLE, Aimee, Joanna; LYNAM, Jason, Martin; WALTON, Paul, Howard; WO2013/38134; (2013); A1;,
Highly efficient and robust molecular ruthenium catalysts for water oxidation
Catalysts | Special Issue : Ruthenium Catalysts – MDPI

301224-40-8, (1,3-Dimesitylimidazolidin-2-ylidene)(2-isopropoxybenzylidene)ruthenium(VI) chloride is a ruthenium-catalysts compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated

Take Grubbs-HoveydaII catalyst (464.0mg, 0.74mmol),Compound II (201.0 mg, 0.9 mmol,) prepared in Example 1 was placed in a 25 mL round bottom flask.Add 15 mL of dry THF and stir at 800 r / min at room temperature for 30 min.After the reaction was completed, the solvent was dried with a vacuum pump to obtain a brown-red solid.Add n-hexane to the solid and stir thoroughly. At this time, the color of n-hexane will turn red. Centrifuge the mixture, discard the liquid, and dry the solid.Compound III (385 mg, yield: 70.6%) was obtained as a brown solid powder.

As the paragraph descriping shows that 301224-40-8 is playing an increasingly important role.

Reference£º
Patent; Jilin Chemical College; Yu Xiaobo; Geng Shudong; Liu Guanchen; (14 pag.)CN110563769; (2019); A;,
Highly efficient and robust molecular ruthenium catalysts for water oxidation
Catalysts | Special Issue : Ruthenium Catalysts – MDPI

246047-72-3, (1,3-Bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene)dichloro(phenylmethylene)(tricyclohexylphosphine)ruthenium is a ruthenium-catalysts compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated

After a 50 mL two-necked flask was purged with argon, the ligand 3bj (10 mmol), CuCl (30 mmol, 3 eq) and 30 mL of dry DCM were successively added and the mixture was purged three times with argon to protect the closed system with an 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 prepare a sand product. The crude product was obtained by silica gel column chromatography and then washed with methanol or pentane-DCM to obtain a green solid product 4bj. Yield: 64%.

As the paragraph descriping shows that 246047-72-3 is playing an increasingly important role.

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