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Journal articles on the topic 'Ru(p-cym)'

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Published: 2 June 2025

Last updated: 31 July 2025

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1

Matveevskaya, Vladislava V., Dmitry I. Pavlov, Denis G. Samsonenko, et al. "Synthesis and Structural Characterization of Half-Sandwich Arene–Ruthenium(II) Complexes with Bis(imidazol-1-yl)methane, Imidazole and Benzimidazole." Inorganics 9, no. 5 (2021): 34. http://dx.doi.org/10.3390/inorganics9050034.

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Mono- and binuclear arene–ruthenium(II) complexes with imidazole-containing ligands were prepared by the reaction of the ligands (L1 = bis(imidazole-1-yl)methane; ImH = 1H-Imidazole; BImH = 1H-Benzimidazole) with [(p-cym)Ru(µ-Cl)2]2 dimers. When bis(imidazole-1-yl)methane reacted with [(p-cym)Ru(µ-Cl)2]2 in methanol, a binuclear complex of the type [Ru2(L1)2(p-cym)2Cl2]Cl2 (2) with cyclic structure was synthesized, whereas by using acetonitrile as a solvent under the same reaction conditions, an unexpected C–N bond cleavage was observed, and a complex of formula [Ru(ImH)2(p-cym)Cl]Cl (1) with

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2

Nolla-Saltiel, Roberto, Ana M. Geer, Helen R. Sharpe, et al. "Organoruthenium Complexes Containing Phosphinodicarboxamide Ligands." Inorganics 11, no. 9 (2023): 372. http://dx.doi.org/10.3390/inorganics11090372.

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Ruthenium complexes of phosphinocarboxamide ligands, and their use to form metallacycles using halide abstraction/deprotonation reactions are reported. Thus, [Ru(p-cym){PPh2C(=O)NHR}Cl2; R = iPr (1), Ph (2), p-tol (3)] and [Ru(p-cym){PPh2C(=O)N(R)C(=O)N(H)R}Cl2; R = Ph (4), p-tol (5)] were synthesized from [(p-cym)RuCl2]2 (p-cym = para-cymene) and phosphinocarboxamides or phosphinodicarboxamides, respectively. Single-crystal X-ray diffraction measurements on 1–5 reveal coordination to ruthenium through the phosphorus donor, with an intramolecular hydrogen bond between the amine-bound proton an

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3

Tran, Tan Ba, Éva Sipos, Attila Csaba Bényei, Sándor Nagy, István Lekli, and Péter Buglyó. "Synthesis and Characterization of Novel Co(III)/Ru(II) Heterobimetallic Complexes as Hypoxia-Activated Iron-Sequestering Anticancer Prodrugs." Molecules 29, no. 24 (2024): 5967. https://doi.org/10.3390/molecules29245967.

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Heterobimetallic complexes of an ambidentate deferiprone derivative, 3-hydroxy-2-methyl-1-(3-((pyridin-2-ylmethyl)amino)propyl)pyridin-4(1H)-one (PyPropHpH), incorporating an octahedral [Co(4N)]3+ (4N = tris(2-aminoethyl)amine (tren) or tris(2-pyridylmethyl)amine (tpa)) and a half-sandwich type [(η6-p-cym)Ru]2+ (p-cym = p-cymene) entity have been synthesized and characterized by various analytical techniques. The reaction between PyPropHpH and [Co(4N)Cl]Cl2 resulted in the exclusive (O,O) coordination of the ligand to Co(III) yielding [Co(tren)PyPropHp](PF6)2 (1) and [Co(tpa)PyPropHp](PF6)2 (2

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4

Tripathy, Suman Kumar, Margarethe van der Meer, Anupam Sahoo та ін. "A dinuclear [{(p-cym)RuIICl}2(μ-bpytz˙−)]+ complex bridged by a radical anion: synthesis, spectroelectrochemical, EPR and theoretical investigation (bpytz = 3,6-bis(3,5-dimethylpyrazolyl)1,2,4,5-tetrazine; p-cym = p-cymene)". Dalton Transactions 45, № 31 (2016): 12532–38. http://dx.doi.org/10.1039/c6dt01995a.

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5

Volkov, Oleg, Nigam P. Rath, and Lawrence Barton. "Chemistry on the Rhodacarborane Cluster [9,9-(PPh3)-nido-9,7,8-RhC2B8H11]: Formation of Bidentate Phosphine and Bimetallic Derivatives." Collection of Czechoslovak Chemical Communications 67, no. 6 (2002): 769–82. http://dx.doi.org/10.1135/cccc20020769.

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The electronically unsaturated rhodacarborane [9,9-(PPh3)2-nido-9,7,8-RhC2B8H11] (1), reacts with Ph2PCH2PPh2 (dppm) to afford [9,9-(dppm-κ2P)-9-(dppm-κP)-nido-9,7,8-RhC2B8H11] (3), in which the Rh-bonded PPh3 ligands have been replaced by two dppm ligands, one in a bidentate mode and the second in a unidentate mode with a free PPh2 end. The structure of 3 is similar to the related, and isoelectronic, species [8,8-(dppm-κ2P)-8-(dppm-κP)-nido-8,7-RhSB9H10] (4), but with a difference in the orientation of the ligands. Reaction of 1 with Ph2P(CH2)2PPh2 (dppe) affords a species tentatively identif

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6

Purkait, Kallol, Subhendu Karmakar, Sudipta Bhattacharyya, Saptarshi Chatterjee, Suman Kr Dey, and Arindam Mukherjee. "A hypoxia efficient imidazole-based Ru(ii) arene anticancer agent resistant to deactivation by glutathione." Dalton Transactions 44, no. 13 (2015): 5969–73. http://dx.doi.org/10.1039/c4dt03983a.

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7

Tripathy, Suman Kumar, Ashoka Chary Taviti, Niranjan Dehury, et al. "Synthesis, characterisation and antibacterial activity of [(p-cym)RuX(L)]+/2+ (X = Cl, H2O; L = bpmo, bpms) complexes." Dalton Transactions 44, no. 11 (2015): 5114–24. http://dx.doi.org/10.1039/c4dt03647f.

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8

Mansour, Ahmed M., and Krzysztof Radacki. "Experimental and DFT studies of sulfadiazine ‘piano-stool’ Ru(ii) and Rh(iii) complexes." RSC Advances 10, no. 18 (2020): 10673–80. http://dx.doi.org/10.1039/d0ra01085e.

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Binding of certain metal complexes to proteins may cause cytotoxicity. While [(η<sup>6</sup>-p-Cym)Ru(L<sup>SZ</sup>)<sub>2</sub>] decomposed during the reaction with hen white egg lysozyme, a Rh(iii) analogue was covalently bio-conjugated via the elimination of a sulfadiazine.

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9

Tripathy, Suman Kumar, Umasankar De, Niranjan Dehury, Satyanarayan Pal, Hyung Sik Kim та Srikanta Patra. "Dinuclear [{(p-cym)RuCl}2(μ-phpy)](PF6)2 and heterodinuclear [(ppy)2Ir(μ-phpy)Ru(p-cym)Cl](PF6)2 complexes: synthesis, structure and anticancer activity". Dalton Trans. 43, № 39 (2014): 14546–49. http://dx.doi.org/10.1039/c4dt01033g.

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10

Ywaya, David O., Halliru Ibrahim, Holger B. Friedrich та ін. "Chemotherapeutic Activities of New η6-p-Cymene Ruthenium(II) and Osmium(II) Complexes with Chelating SS and Tridentate SNS Ligands". Molecules 29, № 5 (2024): 944. http://dx.doi.org/10.3390/molecules29050944.

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A series of new chelating bidentate (SS) alkylimidazole-2-thione-Ru(II)/Os(II) complexes (3ai, 3aii, 3aiii, 3bii/4aiii, 4bi, 4bii), and the tridentate (SNS) pyridine-2,6-diylimidazole-2-thione-Ru(II)/Os(II) complexes (5bi, 5civ/6bi, 6ci, 6civ) in the forms [MII(cym)(L)Cl]PF6 and [MII(cym)(L)]PF6 (M = Ru or Os, cym = η6-p-cymene, and L = heterocyclic derivatives of thiourea) respectively, were successfully synthesized. Spectroscopic and analytical methods were used to characterize the complexes and their ligands. Solid-state single-crystal X-ray diffraction analyses revealed a “piano-stool” geo

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11

Arshad, Jahanzaib, Kelvin K. H. Tong, Sanam Movassaghi, et al. "Impact of the Metal Center and Leaving Group on the Anticancer Activity of Organometallic Complexes of Pyridine-2-carbothioamide." Molecules 26, no. 4 (2021): 833. http://dx.doi.org/10.3390/molecules26040833.

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RuII(cym)Cl (cym = η6-p-cymene) complexes of pyridinecarbothioamides have shown potential for development as orally active anticancer metallodrugs, underlined by their high selectivity towards plectin as the molecular target. In order to investigate the impact of the metal center on the anticancer activity and their physicochemical properties, the Os(cym), Rh- and Ir(Cp*) (Cp* = pentamethylcyclopentadienyl) analogues of the most promising and orally active compound plecstatin 2 were prepared and characterized by spectroscopic techniques and X-ray diffraction analysis. Dissolution in aqueous me

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12

Dimić, Dušan, Thomas Eichhorn, Dejan Milenković, and Goran N. Kaluđerović. "Synthesis, Structural, and Quantum Chemical Analysis of Neutral and Cationic Ruthenium(II) Complexes with Nicotinate-Polyethylene Glycol Ester Ligands." Inorganics 11, no. 12 (2023): 460. http://dx.doi.org/10.3390/inorganics11120460.

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Ruthenium(II/III)-based compounds have gained significant interest due to the biocompatibility of ruthenium, its similarity to iron, and the possibility for structural diversification through the choice of ligands. In this contribution, two novel ligands, (2-(2-methoxyethoxy)ethyl nicotinate hydrochloride) and (2-[2-(2-methoxyethoxy)ethoxy]ethyl nicotinate hydrochloride) (pyCOO(CH2CH2O)nCH3: L2, n = 2; L3, n = 3), were synthesized and characterized via ESI-HRMS, as well as IR and NMR spectroscopies. Their structures were optimized at the B3LYP/6-311++G(d,p) level of theory, and NMR chemical sh

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13

Thomas, Rhodri Ll, and Lawrence Barton. "[4-{(p-cym)Ru}-5-{(Ph3P)2(CO)Os}B4H8]: the first nido-heterobimetallahexaborane cluster." Inorganica Chimica Acta 289, no. 1-2 (1999): 134–40. http://dx.doi.org/10.1016/s0020-1693(99)00063-8.

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14

Bihari, Zsolt, Valeria Ugone, Eugenio Garribba, Norbert Lihi та Péter Buglyó. "Complex formation between [(η6-p-cym)Ru(H2O)3]2+ and oligopeptides containing three histidyl moieties". Journal of Organometallic Chemistry 823 (листопад 2016): 116–25. http://dx.doi.org/10.1016/j.jorganchem.2016.09.013.

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15

Nagy, Sándor, András Ozsváth, Attila Cs Bényei, Etelka Farkas, and Péter Buglyó. "Donor Atom Preference of Organoruthenium and Organorhodium Cations on the Interaction with Novel Ambidentate (N,N) and (O,O) Chelating Ligands in Aqueous Solution." Molecules 26, no. 12 (2021): 3586. http://dx.doi.org/10.3390/molecules26123586.

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Two novel, pyridinone-based chelating ligands containing separated (O,O) and (Namino,Nhet) chelating sets (Namino = secondary amine; Nhet = pyrrole N for H(L3) (1-(3-(((1H-pyrrole-2-yl)methyl)-amino)propyl)-3-hydroxy-2-methylpyridin-4(1H)-one) or pyridine N for H(L5) (3-hydroxy-2-methyl-1-(3-((pyridin-2-ylmethyl)amino)propyl)pyridin-4(1H)-one)) were synthesized via reduction of the appropriate imines. Their proton dissociation processes were explored, and the molecular structures of two synthons were assessed by X-ray crystallography. These ambidentate chelating ligands are intended to develop

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16

Bíró, Linda, Botond Tóth, Norbert Lihi, Etelka Farkas та Péter Buglyó. "Interaction between [(η6-p-cym)M(H2O)3]2+ (MII = Ru, Os) or [(η5-Cp*)M(H2O)3]2+ (MIII = Rh, Ir) and Phosphonate Derivatives of Iminodiacetic Acid: A Solution Equilibrium and DFT Study". Molecules 28, № 3 (2023): 1477. http://dx.doi.org/10.3390/molecules28031477.

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The pH-dependent binding strengths and modes of the organometallic [(η6-p-cym)M(H2O)3]2+ (MII = Ru, Os; p-cym = 1-methyl-4-isopropylbenzene) or [(η5-Cp*)M(H2O)3]2+ (MIII = Rh, Ir; Cp* = pentamethylcyclopentadienyl anion) cations towards iminodiacetic acid (H2Ida) and its biorelevant mono- and diphosphonate derivatives N-(phosphonomethyl)-glycine (H3IdaP) and iminodi(methylphosphonic acid) (H4Ida2P) was studied in an aqueous solution. The results showed that all three of the ligands form 1:1 complexes via the tridentate (O,N,O) donor set, for which the binding mode was further corroborated by t

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17

McQuade, Paul, Nigam P. Rath, and Lawrence Barton. "[BH3·PPh2CH2C6H4CH2PPh2·Ru(p-cym)Cl2]: A New Bifunctional Compound and Prototype of a Linked Borane/Metal Cluster Species." Inorganic Chemistry 38, no. 23 (1999): 5468–70. http://dx.doi.org/10.1021/ic990687s.

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18

Freixa, Zoraida, and María Angeles Garralda. "Insights into the use of [Ru(p-Cym)(bipy)Cl]Cl as precatalyst for solvolytic dehydrogenation of ammonia-borane." Inorganica Chimica Acta 431 (May 2015): 184–89. http://dx.doi.org/10.1016/j.ica.2014.12.005.

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19

Bíró, Linda, Etelka Farkas та Péter Buglyó. "Hydrolytic behaviour and chloride ion binding capability of [Ru(η6-p-cym)(H2O)3]2+: a solution equilibrium study". Dalton Trans. 41, № 1 (2012): 285–91. http://dx.doi.org/10.1039/c1dt11405k.

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20

Janković, Nenad, Goran Bogdanović, Nevenka Gligorijević та ін. "Novel organoruthenium complexes containing β-Diketonates: Synthesis, characterization, DNA/HSA interactions, and the impact of biocompatible ionic liquids on biological activities". Journal of Inorganic Biochemistry 270 (23 травня 2025): 112941. https://doi.org/10.1016/j.jinorgbio.2025.112941.

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In order to discover new dual-active agents, novel ruthenium (η6-p-cymene) complexes of the general formula [(η6-p-cym)Ru(O–O)Cl] with O,O-diketo ester ligands ethyl 2-hydroxy-4-aryl-4-oxobut-2-enoate (1–3), were synthesized. The complexes 1–3 were characterized by spectral techniques (UV–Vis, IR, 1H and 13C NMR, andESI-HRMS), elemental analysis, and X-ray crystallography. Based on in vitro DNA/HSA experiments, complex 1 exhibited the highest DNA/HSA-activity, suggesting that the presence of an alkene chain contributes to increased activity. The cytotoxic activi

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21

Bíró, Linda, Etelka Farkas та Péter Buglyó. "Complex formation between Ru(η6-p-cym)(H2O)3]2+ and (O,O) donor ligands with biological relevance in aqueous solution". Dalton Transactions 39, № 42 (2010): 10272. http://dx.doi.org/10.1039/c0dt00469c.

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22

Bíró, Linda, Dániel Hüse, Attila Cs Bényei та Péter Buglyó. "Interaction of [Ru(η6-p-cym)(H2O)3]2+ with citrate and tricarballate ions in aqueous solution; X-ray crystal structure of novel half-sandwich Ru(II)-citrato complexes". Journal of Inorganic Biochemistry 116 (листопад 2012): 116–25. http://dx.doi.org/10.1016/j.jinorgbio.2012.07.020.

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23

Ozsváth, Bíró, Nagy, Buglyó, Sanna, and Farkas. "Trends and Exceptions in the Interaction of Hydroxamic Acid Derivatives of Common Di- and Tripeptides with Some 3d and 4d Metal Ions in Aqueous Solution." Molecules 24, no. 21 (2019): 3941. http://dx.doi.org/10.3390/molecules24213941.

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By using various techniques (pH-potentiometry, UV-Visible spectrophotometry, 1H and 17O-NMR, EPR, ESI-MS), first time in the literature, solution equilibrium study has been performed on complexes of dipeptide and tripeptide hydroxamic acids—AlaAlaNHOH, AlaAlaN(Me)OH, AlaGlyGlyNHOH, and AlaGlyGlyN(Me)OH—with 4d metals: the essential Mo(VI) and two half-sandwich type cations, [(η6-p-cym)Ru(H2O)3]2+ as well as [(η5-Cp*)Rh(H2O)3]2+, the latter two having potential importance in cancer therapy. The tripeptide derivatives have also been studied with some biologically important 3d metals, such as Fe(

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24

Bihari, Zsolt, Zoltán Nagy та Péter Buglyó. "[(η6-p-cym)Ru(H2O)3]2+ binding capability of N-methylimidazole to model the interaction between the metal ion and surface histidine residues of peptides". Journal of Organometallic Chemistry 782 (квітень 2015): 82–88. http://dx.doi.org/10.1016/j.jorganchem.2014.12.026.

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25

Bíró, Linda, Péter Buglyó, and Etelka Farkas. "Diversity in the Interaction of Amino Acid- and Peptide-Based Hydroxamic Acids with Some Platinum Group Metals in Solution." Molecules 27, no. 3 (2022): 669. http://dx.doi.org/10.3390/molecules27030669.

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Complexes that incorporate both ligand(s) and metal(s) exhibiting cytotoxic activity can especially be interesting to develop multifunctional drug molecules with desired activities. In this review, the limited number of solution results collected in our laboratory on the complexes of Pd(II) and two other platinum group metals—the half-sandwich type, [(η6-p-cym)Ru(H2O)3]2+, and [(η5-Cp*)Rh(H2O)3]2+—with hydroxamic acid derivatives of three amino acids, two imidazole analogues, and four small peptides are summarized and evaluated. Unlike the limited number of coordination sites of these metal io

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26

Bíró, Linda, Edina Balogh та Péter Buglyó. "Interaction between [Ru(η6-p-cym)(H2O)3]2+ and dl-serine or dl-isoserine: The role of the side chain alcoholic OH group in metal ion binding". Journal of Organometallic Chemistry 734 (червень 2013): 61–68. http://dx.doi.org/10.1016/j.jorganchem.2012.11.023.

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27

Heinzel, Ulrich, Andreas Henke, and Rainer Mattes. "Main-group and transition-metal complexes of 1-thia-4,7-diazacyclononane, [9]aneN2S. Crystal structures of [VOCl2([9]aneN2S)]· MeCN, [Fe([9]aneN2S)2][ClO4]2, [Zn([9]aneN2S)2][PF6]2, [Ru(cym)([9]aneN2S)][BPh4]Cl2·M eCN (cym = p-cymene), [RhCl3([9]aneN2S)]·H2O and [Tl([9]aneN2S)][ClO4]." Journal of the Chemical Society, Dalton Transactions, no. 4 (1997): 501–8. http://dx.doi.org/10.1039/a605999f.

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28

Georgakopoulou, Christina, Dimitrios Thomos, Theodoros Tsolis та ін. "Synthesis, characterization, interactions with the DNA duplex dodecamer d(5΄-CGCGAATTCGCG-3΄)2 and cytotoxicity of binuclear η6-arene-Ru(II) complexes." Dalton Transactions, 2022. http://dx.doi.org/10.1039/d2dt02304k.

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The novel binuclear η6-arene-Ru(II) complexes with the general formula {[(η6-cym)Ru(L)]2(μ-BL)}(PF6)4, and their corresponding water soluble {[(η6-cym)Ru(L)]2(μ-BL)}Cl4, where cym = p-cymene, L = 2,2΄-bipyridine (bpy) and 1,10-phenanthroline (phen), BL = 4,4΄-bipyridine...

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29

Lamata, Pilar, Sophie Beard, Alejandro Grasa, et al. "Molecular hydrogen and water activation by transition metal frustrated Lewis pairs containing ruthenium or osmium components: catalytic hydrogenation assays." Dalton Transactions, 2023. http://dx.doi.org/10.1039/d3dt02339g.

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The transition metal frustrated Lewis pair compounds [(Cym)M(κ3S,P,N-HL1)][SbF6] (Cym = η6-p-MeC6H4iPr; H2L1 = N-(p-Tolyl)-N’-(2-diphenylphosphanoethyl)thiourea ; M = Ru (5), Os (6)) have been prepared from the corresponding dimer [{(Cym)MCl}2(μ-Cl)2] and...

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30

Kumar, Saawan, Mie Riisom, Stephen M. F. Jamieson, et al. "Expanding on the plecstatin anticancer agent class: exchange of the chlorido ligand for N-heterocyclic ligands." Australian Journal of Chemistry 77, no. 9 (2024). http://dx.doi.org/10.1071/ch24080.

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Metal piano-stool complexes based on pyridinecarbothioamide (PCA) have shown promising antiproliferative and in vivo anticancer activity, in particular [Ru(cym)(p-F-PCA)Cl]PF6 (cym is η6-p-cymene; plecstatin-1). The impact of modifications of the PCA and π-bound ligands on biological properties has been extensively investigated. Herein, we explored the influence of exchanging the chlorido ligand with the N-heterocycles 1-methylimidazole, 1-methylbenzimidazole and pyridine. In solution, an equilibrium between the protonated and deprotonated forms of the thioamide bond was observed, which was fo

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31

Wang, Runbao, Rong Zhang, Kun Jin, Yaming Li, Chunying Duan, and Liang Zhao. "Ruthenium(II)-Catalyzed C-H Allylation of N,N-Dialkyl Thiobenzamides with Allyl Methyl Carbonate by Sulfur Coordination." Synlett, September 13, 2024. http://dx.doi.org/10.1055/a-2415-3708.

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This report describes the Ru(II)-catalyzed C-H allylation of N,N-dialkyl thiobenzamides with allyl carbonate. The reaction is carried out using [RuCl2(p-cym)]2 in the presence of Cu(OAc)2 and Ag2O. This method represents the first example of Ru-catalyzed C-H allylation directed by sulfur-containing groups. As a further advantage, the method is performed in sustainable and eco-friendly MeCN as a solvent.

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32

Riisom, Mie, Liam Eade, William D. J. Tremlett, and Christian G. Hartinger. "The aqueous stability and interactions of organoruthenium compounds with serum proteins, cell culture medium and human serum." Metallomics, June 25, 2022. http://dx.doi.org/10.1093/mtomcs/mfac043.

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Abstract Metal complexes bind to a wide variety of biomolecules and the control of the reactivity is essential when designing anticancer metallodrugs with a specific mode of action in mind. In this study, we used the highly cytotoxic compound [RuII(cym)(8-HQ)Cl] (cym = η6-p-cymene, 8-HQ = 8-hydroxyquinoline), the more inert derivative [RuII(cym)(8-HQ)(PTA)](SO3CF3) (PTA = 1,3,5-triaza-7-phosphaadamantane), and [RuII(cym)(PCA)Cl]Cl (PCA = pyridinecarbothioamide) as a derivative with a different coordination environment about the Ru center and investigated their stability, interactions with prot

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33

Ge, Shun, Jia-Hao Liu, Lishan Gong, et al. "Dehydrogenation of Aqueous Formic Acid by Iridium and Ruthenium Complexes with Nitrogen‐rich Diamino‐bis(1H‐1,2,4‐triazole)." European Journal of Inorganic Chemistry, November 9, 2023. http://dx.doi.org/10.1002/ejic.202300509.

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The development of efficient catalysts for the dehydrogenation of formic acid (FA) through molecular level control and precise regulation remains challenging. Herein, we report the newly developed complexes of iridium and ruthenium with nitrogen‐rich ligand for aqueous FA dehydrogenation. The Cp*Ir complex 1 (Cp*= cyclopentadienyl) and Ru(p‐cym) complex 2 (p‐cym= p‐Cymene) were synthesized and fully characterized. The single crystal structures of these complexes have a typical piano‐stool structure. A turnover frequency of 12468 h−1 was achieved for FA dehydrogenation at 90 °C by using complex

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34

Riisom, Mie, Stephen M. F. Jamieson, and Christian G. Hartinger. "Critical Evaluation of Cell Lysis Methods for Metallodrug Studies in Cancer Cells." Metallomics, August 18, 2023. http://dx.doi.org/10.1093/mtomcs/mfad048.

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Abstract Intracellular accumulation studies are a key step in metallodrug development but often variable results are obtained. Therefore, we aimed here to investigate different protocols for efficient and reproducible lysis of cancer cells in terms of protein content in lysates and in cell uptake studies of the Ru anticancer complex [chlorido(8-oxyquinolinato)(η6-p-cymene)ruthenium(II)] ([Ru(cym)(HQ)Cl]). The physical lysis methods osmosis and sonication were chosen for comparison with chemical lysis with the radioimmunoprecipitation assay buffer (RIPA). Based on the protein content and the to

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35

Manzano, Blanca Rosa, Carlos Gonzalo-Navarro, Margarita Ruiz-Castañeda, Jairo Fidalgo, Gustavo Espino, and Félix A. Jalón. "Ruthenium Catalysed Transfer Deuteration of Heteroaromatics in D2O." Asian Journal of Organic Chemistry, October 24, 2024. http://dx.doi.org/10.1002/ajoc.202400462.

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There is a growing interest in deuterated derivatives in various fields, including the pharmaceutical industry. In this industry, partially hydrogenated heterocycles are also a target. Combining these two concepts, it was studied the reduction of heterocycles with simultaneous deuterium incorporation by transfer deuteration, a process of introducing two deuterium atoms into an organic molecule using non‐D2 sources, avoiding the use of a gas or harmful reagents. Formic acid/sodium formate and D2O as the sole deuterium source were used under mild conditions. The precatalyst was [RuCl(p‐cym)(dmbp

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Patil, Rahul Daga, Sandip Bapu Khatal, Manohar Shivaji Padmor, and Sanjay Pratihar. "Waste-Minimized, Ecofriendly, and Chemoselective Room-Temperature Hydrogenation of C=C Bonds Using a Homogeneous Recyclable Imidazole-Based Ru(II)-p-Cym Catalyst." Green Chemistry, 2025. https://doi.org/10.1039/d5gc01274k.

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Catalytic hydrogenation of C=C bonds is crucial in fine chemical and pharmaceutical synthesis, yet the efficient recovery and reuse of homogeneous catalysts remain a challenge. Herein, we report a well-defined...

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37

Patil, Rahul Daga, Amishwar Raysing Shelte, Ankush V. Biradar, and Sanjay Pratihar. "Sustainable and selective transfer hydrogenation using waste shrimp shell‐based tetrazene‐Ru (II) para‐cymene catalyst with ethanol as a hydrogen source." Applied Organometallic Chemistry, August 22, 2023. http://dx.doi.org/10.1002/aoc.7221.

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Sustainable chemical research emphasizes chitosan‐based catalysts and the need to explore the direct utilization of waste shrimp shells, whereas the use of ethanol as a hydrogen source in transfer hydrogenation is less explored due to its unfavorable redox potential, higher energy barriers, generation of reactive intermediates, and catalyst poising via metal carbonyl species or decarbonylation. Herein, we disclosed an efficient synthetic approach, conducted at ambient temperature, for surface functionalization of waste shrimp shells with 3‐(3,5‐dimethyl‐1H‐pyrazol‐1‐yl)‐1,2,4,5‐tetrazine (DMPZ

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