Category: 50982-12-2

As a common heterocyclic compound, it belongs to ruthenium-catalysts compound, name is Dichloro(cycloocta-1,5-diene)ruthenium(II), and cas is 50982-12-2, its synthesis route is as follows.

General procedure: The following common procedure was followed for the synthesesof complexes 1-5: A mixture of the ligand (0.36 mmol) and Ru(1,5-cod)Cl2(0.36 mmol) was dissolved in dry ethanol (10 ml) and the resultingmixture was refluxed for 2 h. The reaction volume was concentratedto a third of its original volume and the suspension was keptat 4 C overnight to give brick red solid which was filtered off,washed with cold ethanol and then diethyl ether. The solid wasdissolved in chloroform and excess of n-hexane was added toinduce the precipitation of the brick red solid product.

50982-12-2, In the field of chemistry, the synthetic routes of compounds are constantly being developed and updated. I will also mention this compound in other articles.,50982-12-2 ,Dichloro(cycloocta-1,5-diene)ruthenium(II), other downstream synthetic routes, hurry up and to see

Reference£º
Article; Thangavel, Saravanan; Rajamanikandan, Ramar; Friedrich, Holger B.; Ilanchelian, Malaichamy; Omondi, Bernard; Polyhedron; vol. 107; (2016); p. 124 – 135;,
Highly efficient and robust molecular ruthenium catalysts for water oxidation
Catalysts | Special Issue : Ruthenium Catalysts – MDPI

50982-12-2, In the next few decades, the world population will flourish. As the population grows rapidly and people all over the world use more and more resources, all industries must consider their environmental impact. Dichloro(cycloocta-1,5-diene)ruthenium(II), cas is 50982-12-2,the ruthenium-catalysts compound, it is a common compound, a new synthetic route is introduced below.

Toluene (5 ml) was added to a mixture of (Ad2PCH2CH2)2NH (250 mg, 0.37 mmol) and [RuCl2(cod)]n (104 mg, 0.37 mmol) under argon and the mixture refluxed for 20 hours. The mixture was cooled to room temperature and4-methoxyphenyl isonitrile (49 mg, 0.37 mmol) added and the mixture refluxed for 12 hours under argon. It was cooled to room temperature and ether (40 ml) added. The pale brown solid was filtered, washed with ether and dried under vacuum. Yield = 0.18 g.

Chemical properties determine the actual use. Each compound has specific chemical properties and uses. We look forward to more synthetic routes in the future to expand reaction routes of Dichloro(cycloocta-1,5-diene)ruthenium(II), 50982-12-2

Reference£º
Patent; HADEED, Gerald, S.; ABDUR-RASHID, Kamaluddin; (61 pag.)WO2018/193401; (2018); A1;,
Highly efficient and robust molecular ruthenium catalysts for water oxidation
Catalysts | Special Issue : Ruthenium Catalysts – MDPI

Researchers who often do experiments know that organic synthesis is a process of preparing more complex target molecules from simple raw materials through one or more chemical reactions. Generally, it requires fewer steps, and cheap raw materials.50982-12-2, name is Dichloro(cycloocta-1,5-diene)ruthenium(II) A new synthetic method of this compound is introduced below., 50982-12-2

50982-12-2, Toluene (5 ml) was added to a mixture of (Ad2PCH2CH2)2NH (250 mg, 0.37 mmol) and [RuCl2(cod)]n (104 mg, 0.37 mmol) under argon and the mixture refluxed for 20 hours. The mixture was cooled to room temperature and4-methoxyphenyl isonitrile (49 mg, 0.37 mmol) added and the mixture refluxed for 12 hours under argon. It was cooled to room temperature and ether (40 ml) added. The pale brown solid was filtered, washed with ether and dried under vacuum. Yield = 0.18 g.

50982-12-2 is used more and more widely, we look forward to future research findings about Dichloro(cycloocta-1,5-diene)ruthenium(II)

Reference£º
Patent; HADEED, Gerald, S.; ABDUR-RASHID, Kamaluddin; (61 pag.)WO2018/193401; (2018); A1;,
Highly efficient and robust molecular ruthenium catalysts for water oxidation
Catalysts | Special Issue : Ruthenium Catalysts – MDPI

50982-12-2, In the next few decades, the world population will flourish. As the population grows rapidly and people all over the world use more and more resources, all industries must consider their environmental impact.50982-12-2, Dichloro(cycloocta-1,5-diene)ruthenium(II) it is a common compound, a new synthetic route is introduced below.

A mixture of [RuCl2(COD)]n (309 mg, 1.103 mmol), PCy3 (309 mg, 1.103 mmol) and la (294 mg, 1.103 mmol) was stirred in toluene (10 ml) at 115 C for 48 h in a KONTES pressure tube. After cooling down, the brick colored precipitate was collected on a filter frit, washed with Et20 (3 x 10 ml) and vacuum dried to afford 642 mg of the crude material. To the crude material was added CH2C12 (~ 32 ml) and the obtained mixture was brought to reflux and filtered using a Whatman syringe filter (PTFE membrane, pore size 0.45 muiotaeta). Layering the obtained red-brown solution with Et20 (125 ml) afforded 327 mg (41%) of the product as a pink-brown powder after 5 days. Elem. Anal.: Calcd for C32H55Cl2N2OPRuS (718.81): C, 53.47; H, 7.71; N, 3.90%. Found: C, 53.11; H, 8.00; N, 3.86%. 31P{1H} (162 MHz, CD2C12, r.t.): delta 24.0 (s). 1H NMR (400 MHz, CD2C12, r.t.): delta 0.09 (brs, 1H), 0.92 (brs, 2H), 1.04-1.63 (m, 15H), 1.63-2.05 (m, 9H), 2.10-2.45 (brs, 3H), 2.45-2.70 (brs, 1H), 2.83-3.28 (overlapped, 7H), 3.31-3.56 (overlapped, 6H), 3.56-3.90 (overlapped, 4H), 3.98 (t, J~ 8 Hz, 1H), 5.57 (brs, NH, 1H), 7.31 (t, J~ 7 Hz, 2H), 7.38 (t, J~ 6 Hz, 1H), 8.15 (d, J~ 7 Hz, 2H). 13C{1H} selected for the coordinated NNS ligand (100.5 MHz, CD2C12, r.t.): delta 46.6 (s, 1C), 46.8 (s, 1C), 48.3 (s, 1C), 53.9 (s, 1C, overlapped with CD2C12 peak), 54.8 (s, 1C), 60.0 (s, 1C), 60.7 (s, 1C), 61.7 (s, 1C), 128.1 (s, 2Cmeta, Ph), 129.3 (s, Cpam, Ph), 134.9 (s, 2Cortho, Ph), 138.0 (s, Cipso, Ph).

With the complex challenges of chemical substances, we look forward to future research findings about 50982-12-2,belong ruthenium-catalysts compound

Reference£º
Patent; LOS ALAMOS NATIONAL SECURITY, LLC; DUB, Pavel, A.; GORDON, John, Cameron; WO2015/191505; (2015); A1;,
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 Dichloro(cycloocta-1,5-diene)ruthenium(II), and cas is 50982-12-2, its synthesis route is as follows.

[HNEt3][7,8-nido-C2B9H12] (0.400 g, 1.71 mmol) was suspended in degassed ether (35 mL). n-BuLi (1.40 mL, 3.50 mmol) was added, giving a pale yellow suspension which was stirred under N2 for 1 h, then heated at reflux for 90 min. The resulting solution was filtered, and the ether removed in vacuo to give a yellow oily solid which was subsequently dissolved in degassed THF (35 mL). [RuCl2(COD)]x (0.560 g, 2.00 mmol) and a large excess of naphthalene were added to the THF solution. The resulting brown mixture was heated at reflux for 90 min, then allowed to cool to room temperature. The brown mixture was filtered through a short silica column eluting with DCM to afford a brown solution, removal of solvent from which yielded a brown solid. This was further purified by column chromatography (1:2 DCM:40-60 petroleum ether) giving a yellow band, followed by preparative TLC (2:1 DCM:40-60 petroleum ether). C12H19B9Ru requires: C 39.85, H 5.30. Found: C 39.87, H 5.53%.

50982-12-2, In the field of chemistry, the synthetic routes of compounds are constantly being developed and updated. I will also mention this compound in other articles.,50982-12-2 ,Dichloro(cycloocta-1,5-diene)ruthenium(II), other downstream synthetic routes, hurry up and to see

Reference£º
Article; Scott, Greig; Ellis, David; Rosair, Georgina M.; Welch, Alan J.; Journal of Organometallic Chemistry; vol. 721-722; (2012); p. 78 – 84;,
Highly efficient and robust molecular ruthenium catalysts for water oxidation
Catalysts | Special Issue : Ruthenium Catalysts – MDPI

Name is Dichloro(cycloocta-1,5-diene)ruthenium(II), as a common heterocyclic compound, it belongs to ruthenium-catalysts compound, and cas is 50982-12-2, its synthesis route is as follows.

General procedure: The following common procedure was followed for the synthesesof complexes 1-5: A mixture of the ligand (0.36 mmol) and Ru(1,5-cod)Cl2(0.36 mmol) was dissolved in dry ethanol (10 ml) and the resultingmixture was refluxed for 2 h. The reaction volume was concentratedto a third of its original volume and the suspension was keptat 4 C overnight to give brick red solid which was filtered off,washed with cold ethanol and then diethyl ether. The solid wasdissolved in chloroform and excess of n-hexane was added toinduce the precipitation of the brick red solid product.

50982-12-2, In the field of chemistry, the synthetic routes of compounds are constantly being developed and updated. I will also mention this compound in other articles.,50982-12-2 ,Dichloro(cycloocta-1,5-diene)ruthenium(II), other downstream synthetic routes, hurry up and to see

Reference£º
Article; Thangavel, Saravanan; Rajamanikandan, Ramar; Friedrich, Holger B.; Ilanchelian, Malaichamy; Omondi, Bernard; Polyhedron; vol. 107; (2016); p. 124 – 135;,
Highly efficient and robust molecular ruthenium catalysts for water oxidation
Catalysts | Special Issue : Ruthenium Catalysts – MDPI

50982-12-2, In the next few decades, the world population will flourish. As the population grows rapidly and people all over the world use more and more resources, all industries must consider their environmental impact. Dichloro(cycloocta-1,5-diene)ruthenium(II), cas is 50982-12-2,the ruthenium-catalysts compound, it is a common compound, a new synthetic route is introduced below.

A mixture of [RuCl2(COD)]n (155 mg, 0.552 mmol) and la (147 mg, 0.552 mmol) was stirred in toluene (10 ml) at 115 C for 48 h in Kontes pressure tube. After cooling, a brick-colored precipitate was collected on a filter frit, washed with Et20 (3 x 10 ml) and vacuum dried on the filter. The material was extracted on the filter with 5 x 3 ml CH2C12 allowing the filtrates to be collected in 5 separate vials. A red solution in each vial was layered with Et20 (20 ml). In 1 week, the combined precipitates (or red crystals) from each vial were collected, washed with Et20 (3 x 10 ml) and vacuum-dried to afford 144 mg of the desired product (60%). Elem. Anal: Calcd for C28H44CI4N4O2RU2S2 (876.75): C, 38.36; H, 5.06; N, 6.39%. Found C, 38.38; H, 4.99; N, 6.32%. Elem. Anal: Calcd for C28H44CI4N4O2RU2S2 (876.75): C, 38.36; H, 5.06; N, 6.39%. Found (under nitrogen): C, 38.61; H, 4.99; N, 6.17%. The complex is poorly soluble in CDC13, slightly better in CD2C12. 1H NMR (400 MHz, CD2C12, r.t., saturated): delta 2.00 (brs, 1H), 2.15 (d, J~ 14 Hz, 1H), 2.37 (t, J~ 12 Hz, 1H), 2.15 (m, 4H), 2.75-2.94 (m, 3H), 3.04 (d, J~ 14 Hz, 1H), 3.07-3.23 (m, 5H), 3.38 (m, 2H), 3.44-3.62 (m, 3H), 3.61-3.75 (m, 3H), 3.79 (d, J~ 12 Hz, 1H), 3.87 (t, J~ 14 Hz, 1H), 3.93-4.09 (overlapped m, 3H), 4.06 (brs, 1H), 4.44 (t, J~ 11 Hz, 1H), 4.72 (brs, 1H, possibly NH), 5.07 (d, J~ 18 Hz, 1H), 6.72-8.85 (overlapped, 10H), 9.19 (brs, 1H, NH – C1). The same compound is obtained if the synthesis is carried out in the presence of P(C6F5)3. (0457) [0216] An X-ray structure of complex K-1 revealed that one ligand coordinates to one Ru atom via mer-fashion. A second ligand coordinates to second Ru atom via ^ac-fashion. Both Ru atoms are connected via one bridging CI atom. One S(Ph) atom is part of mer-coordinated la. There appears to be a hydrogen-bonding interaction between one NH group of the fac- coordinated ligand and terminal CI atom attached to the first Ru atom. Complex K-1 exists as a single species in solution. The NH hydrogen atom H-bonded to the chloride ligand appears at delta 9.19 ppm in the 1H NMR spectrum. It is shifted to low field by Deltadelta = 4.47 ppm relative to the NH resonance of the non-H bonded NH group.

Chemical properties determine the actual use. Each compound has specific chemical properties and uses. We look forward to more synthetic routes in the future to expand reaction routes of Dichloro(cycloocta-1,5-diene)ruthenium(II), 50982-12-2

Reference£º
Patent; LOS ALAMOS NATIONAL SECURITY, LLC; DUB, Pavel, A.; GORDON, John, Cameron; WO2015/191505; (2015); A1;,
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 Dichloro(cycloocta-1,5-diene)ruthenium(II), and cas is 50982-12-2, its synthesis route is as follows.

11 g of trimethylsilyl chloride was dissolved in 30 mol of well dried tetrahydrofuran in a 300 ml flask whose inside had been substituted by nitrogen, and the obtained solution was cooled to -78 C. 100 ml of a tetrahydrofuran solution (2.0 mol/l) of cyclopentadienyl sodium was added dropwise to the above solution in a stream of nitrogen over 1 hour. The solution was stirred at -78 C. for 1 hour and returned to room temperature over 6 hours. A salt precipitated in the mixture solution was removed by filtration in a nitrogen atmosphere, and the residual solution was distilled to obtain 8 g of trimethylsilyl cyclopentadiene. 0.5 g of metal sodium was mixed with a well dried tetrahydrofuran solution in a 300 ml flask whose inside had been substituted by nitrogen, and the resulting solution was cooled to -78 C. A solution of 2.5 g of the above synthesized trimethylsilyl cyclopentadiene dissolved in 30 ml of tetrahydrofuran was added dropwise to the above solution in a stream of nitrogen over 1 hour and further heated to room temperature under agitation for 3 hours to obtain a tetrahydrofuran solution of trimethylsilyl cyclopentadienyl sodium. Separately, 5 g of dichloro(cyclooctadienyl)ruthenium was dissolved in 200 ml of well dried tetrahydrofuran in a 500 ml flask whose inside had been substituted by nitrogen. This solution was cooled to -78 C., and the above synthesized tetrahydrofuran solution of trimethylsilyl cyclopentadienyl sodium was added dropwise to the above solution in a stream of nitrogen over 1 hour. The resulting solution was stirred at -78 C. for 3 hours and returned to room temperature under agitation over 12 hours. After the solution was let pass through a neutral alumina column in an argon gas atmosphere to be purified and concentrated, it was separated and purified by a neutral alumina column again to obtain 0.9 g of bis(trimethylsilylcyclopentadienyl)ruthenium (yield rate of 13%).

50982-12-2, In the field of chemistry, the synthetic routes of compounds are constantly being developed and updated. I will also mention this compound in other articles.,50982-12-2 ,Dichloro(cycloocta-1,5-diene)ruthenium(II), other downstream synthetic routes, hurry up and to see

Reference£º
Patent; JSR Corporation; US2006/240190; (2006); A1;,
Highly efficient and robust molecular ruthenium catalysts for water oxidation
Catalysts | Special Issue : Ruthenium Catalysts – MDPI

50982-12-2, In the next few decades, the world population will flourish. As the population grows rapidly and people all over the world use more and more resources, all industries must consider their environmental impact. Dichloro(cycloocta-1,5-diene)ruthenium(II), cas is 50982-12-2,the ruthenium-catalysts compound, it is a common compound, a new synthetic route is introduced below.

The catalyst precursor, preferably [RuCI2(COD)]m (1 eq.) (COD = cis,cis-cycloocta-1 ,5 diene), 1 ,4-bis(diphenylphosphino)butane (1.0-1 .2 eq., preferably 1.0 eq.) and 2-picolylamine (1 .0-1.4 eq., preferably 1.225 eq.) were dissolved in one of the above mentioned solvents, preferably methyl isobutylketone (10-20 ml/g Ru-precursor, preferably 20 ml/g). The mixture was heated to reflux for 3 – 5 hours and then cooled to ambient temperature. The solid precipitate was filtered off and washed with the same solvent that was used for the reaction. A person skilled in the art can determine the cis-/trans- isomeric ratio by NMR. The diastereomeric ratios generated by this method are usually in the range of d.r. (diastereomeric ratio) >98% towards the cis isomer. The same results can be achieved starting with [RuCI2(dmso-KS)3(dmso-KO)], [RuCI2(dmso-KS)4]or [RuCI2(bicyclo[2.2.1 ]hepta- 2,5-diene)]m as precursor

The chemical industry reduces the impact on the environment during synthesis,50982-12-2,Dichloro(cycloocta-1,5-diene)ruthenium(II),I believe this compound will play a more active role in future production and life.

Reference£º
Patent; SYNGENTA PARTICIPATIONS AG; LOTHSCHUETZ, Christian; SAINT-DIZIER, Alexandre Christian; WO2014/166777; (2014); A1;,
Highly efficient and robust molecular ruthenium catalysts for water oxidation
Catalysts | Special Issue : Ruthenium Catalysts – MDPI

50982-12-2, In the next few decades, the world population will flourish. As the population grows rapidly and people all over the world use more and more resources, all industries must consider their environmental impact. Dichloro(cycloocta-1,5-diene)ruthenium(II), cas is 50982-12-2,the ruthenium-catalysts compound, it is a common compound, a new synthetic route is introduced below.

General procedure: The following common procedure was followed for the synthesesof complexes 1-5: A mixture of the ligand (0.36 mmol) and Ru(1,5-cod)Cl2(0.36 mmol) was dissolved in dry ethanol (10 ml) and the resultingmixture was refluxed for 2 h. The reaction volume was concentratedto a third of its original volume and the suspension was keptat 4 C overnight to give brick red solid which was filtered off,washed with cold ethanol and then diethyl ether. The solid wasdissolved in chloroform and excess of n-hexane was added toinduce the precipitation of the brick red solid product.

Chemical properties determine the actual use. Each compound has specific chemical properties and uses. We look forward to more synthetic routes in the future to expand reaction routes of Dichloro(cycloocta-1,5-diene)ruthenium(II), 50982-12-2

Reference£º
Article; Thangavel, Saravanan; Rajamanikandan, Ramar; Friedrich, Holger B.; Ilanchelian, Malaichamy; Omondi, Bernard; Polyhedron; vol. 107; (2016); p. 124 – 135;,
Highly efficient and robust molecular ruthenium catalysts for water oxidation
Catalysts | Special Issue : Ruthenium Catalysts – MDPI