{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,6,13]],"date-time":"2026-06-13T04:43:14Z","timestamp":1781325794241,"version":"3.54.1"},"reference-count":58,"publisher":"Elsevier BV","content-domain":{"domain":["elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Journal of Hazardous Materials"],"published-print":{"date-parts":[[2014,3]]},"DOI":"10.1016\/j.jhazmat.2013.11.045","type":"journal-article","created":{"date-parts":[[2013,11,28]],"date-time":"2013-11-28T09:01:24Z","timestamp":1385629284000},"page":"18-23","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":33,"special_numbering":"C","title":["Complex of 2-(methylthio)aniline with palladium(II) as an efficient catalyst for Suzuki\u2013Miyaura CC coupling in eco-friendly water"],"prefix":"10.1016","volume":"269","author":[{"given":"Gyandshwar K.","family":"Rao","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Arun","family":"Kumar","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Mrinal","family":"Bhunia","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Mahabir P.","family":"Singh","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ajai Kumar","family":"Singh","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"78","reference":[{"key":"10.1016\/j.jhazmat.2013.11.045_bib0005","series-title":"Organometallics in Process Chemistry","first-page":"205","article-title":"Palladium-catalyzed cross-coupling reactions in the synthesis of pharmaceuticals","author":"King","year":"2004"},{"key":"10.1016\/j.jhazmat.2013.11.045_bib0010","first-page":"1","volume":"vol. 219","author":"Miyaura","year":"2002"},{"key":"10.1016\/j.jhazmat.2013.11.045_bib0015","series-title":"Modern Arene Chemistry","first-page":"53","author":"Suzuki","year":"2002"},{"key":"10.1016\/j.jhazmat.2013.11.045_bib0020","doi-asserted-by":"crossref","first-page":"3979","DOI":"10.1016\/j.bmcl.2003.08.059","article-title":"SAR of 3,4-dihydropyrido[3,2-d]pyrimidone p38 inhibitors","volume":"13","author":"Liu","year":"2003","journal-title":"Bioorg. Med. Chem. Lett."},{"key":"10.1016\/j.jhazmat.2013.11.045_bib0025","doi-asserted-by":"crossref","first-page":"3979","DOI":"10.1021\/jm9704098","article-title":"Viracept (nelfinavir mesylate, AG1343): a potent, orally bioavailable inhibitor of HIV-1 protease","volume":"40","author":"Kaldor","year":"1997","journal-title":"J. Med. Chem."},{"key":"10.1016\/j.jhazmat.2013.11.045_bib0030","doi-asserted-by":"crossref","first-page":"5994","DOI":"10.1021\/jo101401z","article-title":"Pd-catalyzed assembly of spirooxindole natural products: a short synthesis of horsfiline","volume":"75","author":"Deppermann","year":"2010","journal-title":"J. Org. Chem."},{"key":"10.1016\/j.jhazmat.2013.11.045_bib0035","doi-asserted-by":"crossref","first-page":"9633","DOI":"10.1016\/S0040-4020(02)01188-2","article-title":"Recent applications of the Suzuki\u2013Miyaura cross-coupling reaction in organic synthesis","volume":"58","author":"Kotha","year":"2002","journal-title":"Tetrahedron"},{"key":"10.1016\/j.jhazmat.2013.11.045_bib0040","series-title":"Total Synthesis of Bioactive Natural Products by Palladium-catalyzed Domino Cyclization of Allenes and Related Compounds","first-page":"1","author":"Inuki","year":"2012"},{"key":"10.1016\/j.jhazmat.2013.11.045_bib0045","doi-asserted-by":"crossref","first-page":"84","DOI":"10.1595\/147106711X558301","article-title":"The 2010 Nobel Prize in chemistry: palladium-catalysed cross-coupling","volume":"55","author":"Colacot","year":"2011","journal-title":"Platinum Metals Rev."},{"key":"10.1016\/j.jhazmat.2013.11.045_bib0050","doi-asserted-by":"crossref","first-page":"4176","DOI":"10.1002\/1521-3773(20021115)41:22<4176::AID-ANIE4176>3.0.CO;2-U","article-title":"Palladium-catalyzed coupling reactions of aryl chlorides","volume":"41","author":"Littke","year":"2002","journal-title":"Angew. Chem. Int. Ed."},{"key":"10.1016\/j.jhazmat.2013.11.045_bib0055","doi-asserted-by":"crossref","first-page":"137","DOI":"10.1016\/S0045-6535(00)00546-4","article-title":"Synthesis of polychlorinated biphenyls (PCBs) using the Suzuki-coupling","volume":"45","author":"Lehmler","year":"2001","journal-title":"Chemosphere"},{"key":"10.1016\/j.jhazmat.2013.11.045_bib0060","doi-asserted-by":"crossref","first-page":"1119","DOI":"10.1016\/S0045-6535(01)00052-2","article-title":"Synthesis of hydroxylated PCB metabolites with the Suzuki-coupling","volume":"45","author":"Lehmler","year":"2001","journal-title":"Chemosphere"},{"key":"10.1016\/j.jhazmat.2013.11.045_bib0065","doi-asserted-by":"crossref","first-page":"4135","DOI":"10.1016\/j.tet.2008.01.003","article-title":"Synthesis of dioxin-like monofluorinated PCBs: for the use as internal standards for PCB analysis","volume":"64","author":"Sott","year":"2008","journal-title":"Tetrahedron"},{"key":"10.1016\/j.jhazmat.2013.11.045_bib0070","doi-asserted-by":"crossref","first-page":"828","DOI":"10.1016\/j.envint.2009.01.013","article-title":"Improved syntheses of non-dioxin-like polychlorinated biphenyls (PCBs) and some of their sulfur-containing metabolites","volume":"36","author":"Telu","year":"2010","journal-title":"Environ. Int."},{"key":"10.1016\/j.jhazmat.2013.11.045_bib0075","doi-asserted-by":"crossref","first-page":"735","DOI":"10.1016\/j.chemosphere.2004.04.035","article-title":"Synthesis of polychlorinated biphenyls and their metabolites with a modified Suzuki-coupling","volume":"56","author":"Kania-Korwel","year":"2004","journal-title":"Chemosphere"},{"key":"10.1016\/j.jhazmat.2013.11.045_bib0080","doi-asserted-by":"crossref","first-page":"1242","DOI":"10.1016\/j.chemosphere.2006.02.029","article-title":"Monofluorinated analogues of polychlorinated biphenyls (F-PCBs): synthesis using the Suzuki-coupling, characterization, specific properties and intended use","volume":"77","author":"Luthe","year":"2009","journal-title":"Chemosphere"},{"key":"10.1016\/j.jhazmat.2013.11.045_bib0085","doi-asserted-by":"crossref","first-page":"1873","DOI":"10.1039\/c2gc35401b","article-title":"An efficient protocol for palladium-catalyzed ligand-free Suzuki\u2013Miyaura coupling in water","volume":"14","author":"Mondal","year":"2012","journal-title":"Green Chem."},{"key":"10.1016\/j.jhazmat.2013.11.045_bib0090","doi-asserted-by":"crossref","first-page":"94","DOI":"10.1016\/j.apcata.2011.02.019","article-title":"Oxadiazoline and ketoimine palladium(II) complexes supported on a chitosan membrane and their catalytic activity for the microwave-assisted Suzuki\u2013Miyaura cross-coupling in water","volume":"397","author":"Lasri","year":"2011","journal-title":"Appl. Catal. A: Gen."},{"key":"10.1016\/j.jhazmat.2013.11.045_bib0095","doi-asserted-by":"crossref","first-page":"5602","DOI":"10.1016\/j.tet.2010.05.092","article-title":"N,N,N\u2032,N\u2032-Tetrakis(2-hydroxyethyl)ethylenediamine palladium(II) complex as efficient catalyst for the Suzuki\u2013Miyaura reaction in water","volume":"66","author":"G\u00fclcemal","year":"2010","journal-title":"Tetrahedron"},{"key":"10.1016\/j.jhazmat.2013.11.045_bib0100","doi-asserted-by":"crossref","first-page":"1311","DOI":"10.1016\/j.ica.2009.12.038","article-title":"[Pd(HQS)2] (HQS=8-hydroxyquinoline-5-sulfonic acid): a highly efficient catalyst for Suzuki\u2013Miyaura cross couplings in water","volume":"363","author":"-Espinosa","year":"2010","journal-title":"Inorg. Chim. Acta"},{"key":"10.1016\/j.jhazmat.2013.11.045_bib0105","first-page":"25","volume":"vol. 1","author":"Cornils","year":"2005"},{"key":"10.1016\/j.jhazmat.2013.11.045_bib0110","unstructured":"W.A. Herrmann, C.-P. Reisinger, P. H\u00e4rter, Heck and other C\u2013C coupling reactions in Ref. 16, 1, pp. 230-238."},{"key":"10.1016\/j.jhazmat.2013.11.045_bib0115","doi-asserted-by":"crossref","first-page":"3095","DOI":"10.1021\/cr030009u","article-title":"Organic reactions in aqueous media with a focus on carbon\u2013carbon bond formations: a decade update","volume":"105","author":"Li","year":"2005","journal-title":"Chem. Rev."},{"key":"10.1016\/j.jhazmat.2013.11.045_bib0120","doi-asserted-by":"crossref","first-page":"4648","DOI":"10.1016\/j.jorganchem.2005.07.053","article-title":"Heck and Suzuki coupling reactions in water using poly(2-oxazoline)s functionalized with palladium carbine complexes as soluble, amphiphilic polymer supports","volume":"690","author":"Sch\u00f6nfelder","year":"2005","journal-title":"J. Organomet. Chem."},{"key":"10.1016\/j.jhazmat.2013.11.045_bib0125","doi-asserted-by":"crossref","first-page":"585","DOI":"10.2174\/1385272053765042","article-title":"Palladium-catalyzed cross-coupling in aqueous media: recent progress and current application","volume":"9","author":"Shaughnessy","year":"2005","journal-title":"Curr. Org. Chem."},{"key":"10.1016\/j.jhazmat.2013.11.045_bib0130","doi-asserted-by":"crossref","first-page":"1827","DOI":"10.1002\/ejoc.200500972","article-title":"Beyond TPPTS: new approaches to the development of efficient palladium-catalyzed aqueous-phase cross-coupling reactions","author":"Shaughnessy","year":"2006","journal-title":"Eur. J. Org. Chem."},{"key":"10.1016\/j.jhazmat.2013.11.045_bib0135","doi-asserted-by":"crossref","first-page":"4324","DOI":"10.1021\/ja00167a032","article-title":"Palladium-catalyzed alkylations in aqueous media","volume":"112","author":"Casalnuovo","year":"1990","journal-title":"J. Am. Chem. Soc."},{"key":"10.1016\/j.jhazmat.2013.11.045_bib0140","doi-asserted-by":"crossref","first-page":"5954","DOI":"10.1039\/c0cc01075h","article-title":"Palladacycle containing nitrogen and selenium: highly active pre-catalyst for the Suzuki\u2013Miyaura coupling reaction and unprecedented conversion into nano-sized Pd17Se15","volume":"46","author":"Rao","year":"2010","journal-title":"Chem. Commun."},{"key":"10.1016\/j.jhazmat.2013.11.045_bib0145","doi-asserted-by":"crossref","first-page":"1931","DOI":"10.1039\/C1DT11695A","article-title":"Palladium(II)-selenated Schiff base complex catalyzed Suzuki\u2013Miyaura coupling: dependence of efficiency on alkyl chain length of ligand","volume":"41","author":"Rao","year":"2012","journal-title":"Dalton Trans."},{"key":"10.1016\/j.jhazmat.2013.11.045_bib0150","doi-asserted-by":"crossref","first-page":"5200","DOI":"10.1039\/c2dt32432f","article-title":"Organosulphur and related ligands in Suzuki\u2013Miyaura CC coupling","volume":"42","author":"Kumar","year":"2013","journal-title":"Dalton Trans."},{"key":"10.1016\/j.jhazmat.2013.11.045_bib0155","doi-asserted-by":"crossref","first-page":"2452","DOI":"10.1021\/om4001956","article-title":"Palladacycles of thioethers catalyzing Suzuki\u2013Miyaura CC coupling: generation and catalytic activity of nanoparticles","volume":"32","author":"Rao","year":"2013","journal-title":"Organometallics"},{"key":"10.1016\/j.jhazmat.2013.11.045_bib0160","doi-asserted-by":"crossref","first-page":"4306","DOI":"10.1039\/c2dt12256a","article-title":"Didocosyl selenide stabilized recyclable Pd(0) nanoparticles and coordinated palladium(II) as efficient catalysts for Suzuki\u2013Miyaura coupling","volume":"41","author":"Rao","year":"2012","journal-title":"Dalton Trans."},{"key":"10.1016\/j.jhazmat.2013.11.045_bib0165","doi-asserted-by":"crossref","first-page":"3533","DOI":"10.1016\/j.jorganchem.2008.07.024","article-title":"Schiff bases of 1\u2032-hydroxy-2\u2032-acetonaphthone containing chalcogen functionalities and their complexes with and (p-cymene)Ru(II), Pd(II), Pt(II) and Hg(II): synthesis, structures and applications in CC coupling reactions","volume":"693","author":"Kumar","year":"2008","journal-title":"J. Organomet. Chem."},{"key":"10.1016\/j.jhazmat.2013.11.045_bib0170","doi-asserted-by":"crossref","first-page":"3208","DOI":"10.1016\/j.ica.2009.02.031","article-title":"Palladium(II), platinum(II), ruthenium(II) and mercury(II) complexes of potentially tridentate Schiff base ligands of (E, N, O) type (E=S, Se, Te): synthesis, crystal structures and applications in Heck and Suzuki coupling reactions","volume":"362","author":"Kumar","year":"2009","journal-title":"Inorg. Chim. Acta"},{"key":"10.1016\/j.jhazmat.2013.11.045_bib0175","doi-asserted-by":"crossref","first-page":"6054","DOI":"10.1021\/om900570g","article-title":"Palladium(II) complexes of the first pincer (Se,N,Se) ligand, 2,6-bis((phenylseleno)methyl)pyridine (L): solvent-dependent formation of [PdCl(L)]Cl and Na[PdCl(L)][PdCl4] and high catalytic activity for the heck reaction","volume":"28","author":"Das","year":"2009","journal-title":"Organometallics"},{"key":"10.1016\/j.jhazmat.2013.11.045_bib0180","doi-asserted-by":"crossref","first-page":"11949","DOI":"10.1039\/c2dt31198d","article-title":"Organoselenium ligands in catalysis","volume":"41","author":"Kumar","year":"2012","journal-title":"Dalton Trans."},{"key":"10.1016\/j.jhazmat.2013.11.045_bib0185","doi-asserted-by":"crossref","first-page":"4852","DOI":"10.1016\/j.poly.2007.09.027","article-title":"Selenated Schiff bases of 2-hydroxyacetophenone and their palladium(II) and platinum(II) complexes: syntheses, crystal structures and applications in the Heck reaction","volume":"27","author":"Kumar","year":"2008","journal-title":"Polyhedron"},{"key":"10.1016\/j.jhazmat.2013.11.045_bib0190","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1016\/j.jorganchem.2013.08.042","article-title":"Palladium(II) complex of an organotellurium ligand as a catalyst for Suzuki\u2013Miyaura coupling: generation and role of nano-sized Pd3Te2","volume":"749","author":"Rao","year":"2014","journal-title":"J. Organomet. Chem."},{"key":"10.1016\/j.jhazmat.2013.11.045_bib0195","doi-asserted-by":"crossref","first-page":"1204","DOI":"10.1021\/om0490278","article-title":"Synthesis of 1-phosphabarrelene phosphine sulfide substituted palladium(II) complexes: application in the catalyzed Suzuki cross-coupling process and in the allylation of secondary amines","volume":"24","author":"Piechaczyk","year":"2005","journal-title":"Organometallics"},{"key":"10.1016\/j.jhazmat.2013.11.045_bib0200","doi-asserted-by":"crossref","first-page":"4403","DOI":"10.1016\/j.tetlet.2006.04.088","article-title":"Microwave-promoted Suzuki\u2013Miyaura cross-coupling of aryl halides with phenylboronic acid under aerobic conditions catalyzed by a new palladium complex with a thiosemicarbazone ligand","volume":"47","author":"Kostas","year":"2006","journal-title":"Tetrahedron Lett."},{"key":"10.1016\/j.jhazmat.2013.11.045_bib0205","doi-asserted-by":"crossref","first-page":"1967","DOI":"10.1016\/j.tetlet.2005.02.003","article-title":"Suzuki\u2013Miyaura cross-coupling reaction of aryl bromides and chlorides with phenylboronic acid under aerobic conditions catalyzed by palladium complexes with thiosemicarbazone ligands","volume":"46","author":"Kostas","year":"2005","journal-title":"Tetrahedron Lett."},{"key":"10.1016\/j.jhazmat.2013.11.045_bib0210","doi-asserted-by":"crossref","first-page":"2642","DOI":"10.1002\/ejic.200600180","article-title":"New palladium complexes with S- or Se-containing Schiff-base ligands as efficient catalysts for the Suzuki\u2013Miyaura cross-coupling reaction of aryl bromides with phenylboronic acid under aerobic conditions","author":"Kostas","year":"2006","journal-title":"Eur. J. Inorg. Chem."},{"key":"10.1016\/j.jhazmat.2013.11.045_bib0215","doi-asserted-by":"crossref","first-page":"4642","DOI":"10.1002\/ejic.200600601","article-title":"Synthesis, characterization, and catalytic applications of palladacyclic complexes bearing C,N,S-donor ligands","author":"Chen","year":"2006","journal-title":"Eur. J. Inorg. Chem."},{"key":"10.1016\/j.jhazmat.2013.11.045_bib0220","doi-asserted-by":"crossref","first-page":"3172","DOI":"10.1039\/b802043d","article-title":"Isolation of an [SNS]Pd(II) pincer with a water ladder and its Suzuki coupling activity in water","author":"Bai","year":"2008","journal-title":"Chem. Commun."},{"key":"10.1016\/j.jhazmat.2013.11.045_bib0225","doi-asserted-by":"crossref","first-page":"4062","DOI":"10.1021\/om8002762","article-title":"Cyclopalladated complexes of 3-thiophosphorylbenzoic acid thioamides: hybrid pincer ligands of a new type. Synthesis, catalytic activity, and photophysical properties","volume":"27","author":"Kozlov","year":"2008","journal-title":"Organometallics"},{"key":"10.1016\/j.jhazmat.2013.11.045_bib0230","doi-asserted-by":"crossref","first-page":"8657","DOI":"10.1039\/b907644a","article-title":"5,6-Membered palladium pincer complexes of 1-thiophosphoryloxy-3-thiophosphorylbenzenes. Synthesis, X-ray structure, and catalytic activity","author":"Kozlov","year":"2009","journal-title":"Dalton Trans."},{"key":"10.1016\/j.jhazmat.2013.11.045_bib0235","doi-asserted-by":"crossref","first-page":"2054","DOI":"10.1021\/om9009894","article-title":"Cyclopalladation of meta-(diphenylthiophosphoryloxy)benzaldimines: NCS and unexpected NCO 5,6-membered pincer palladium complexes","volume":"29","author":"Kozlov","year":"2010","journal-title":"Organometallics"},{"key":"10.1016\/j.jhazmat.2013.11.045_bib0240","doi-asserted-by":"crossref","first-page":"1535","DOI":"10.1039\/c0dt01154a","article-title":"Synthesis, catalytic activity, and photophysical properties of 5,6-membered Pd and Pt SCS\u2032-pincer complexes based on thiophosphorylated 3-amino(hydroxy)benzoic acid thioanilides","volume":"40","author":"Aleksanyan","year":"2011","journal-title":"Dalton Trans."},{"key":"10.1016\/j.jhazmat.2013.11.045_bib0245","doi-asserted-by":"crossref","first-page":"6020","DOI":"10.1021\/om1008023","article-title":"Dinuclear and tetranuclear palladium(II) complexes of a thiolato-functionalized, benzannulated N-heterocyclic carbene ligand and their activities toward Suzuki\u2013Miyaura coupling","volume":"29","author":"Yuan","year":"2010","journal-title":"Organometallics"},{"key":"10.1016\/j.jhazmat.2013.11.045_bib0250","doi-asserted-by":"crossref","first-page":"16939","DOI":"10.1039\/c3dt51658j","article-title":"Palladium(II)-(E,N,E) pincer ligand (E=S\/Se\/Te) complex catalyzed Suzuki coupling reactions in water via in situ generated palladium quantum dots","volume":"42","author":"Kumar","year":"2013","journal-title":"Dalton Trans."},{"key":"10.1016\/j.jhazmat.2013.11.045_bib0255","doi-asserted-by":"crossref","first-page":"1836","DOI":"10.1002\/adsc.200606173","article-title":"Hydrophilic CNC-pincer palladium complexes: a source for highly efficient, recyclable homogeneous catalysts in Suzuki\u2013Miyaura cross-coupling","volume":"348","author":"Churruca","year":"2006","journal-title":"Adv. Synth. Catal."},{"key":"10.1016\/j.jhazmat.2013.11.045_bib0260","first-page":"199","article-title":"Current review on organophosphorus poisoning","volume":"2","author":"Kumar","year":"2010","journal-title":"Arch. Appl. Sci. Res."},{"key":"10.1016\/j.jhazmat.2013.11.045_bib0265","article-title":"Selection of boron reagents for Suzuki\u2013Miyaura coupling","author":"Lennox","year":"2013","journal-title":"Chem. Soc. Rev."},{"key":"10.1016\/j.jhazmat.2013.11.045_bib0270","doi-asserted-by":"crossref","first-page":"13662","DOI":"10.1021\/ja0283899","article-title":"Boronic acids: new coupling partners in room-temperature Suzuki reactions of alkyl bromides. Crystallographic characterization of an oxidative-addition adduct generated under remarkably mild conditions","volume":"124","author":"Kirchhoff","year":"2002","journal-title":"J. Am. Chem. Soc."},{"key":"10.1016\/j.jhazmat.2013.11.045_bib0275","doi-asserted-by":"crossref","DOI":"10.1021\/om4007196","article-title":"Formation and role of palladium chalcogenide and other species in Suzuki\u2013Miyaura and Heck CC coupling reactions catalyzed with palladium(II) complexes of organochalcogen ligands: realities and speculations","author":"Kumar","year":"2013","journal-title":"Organometallics"},{"key":"10.1016\/j.jhazmat.2013.11.045_bib0280","doi-asserted-by":"crossref","first-page":"12552","DOI":"10.1039\/c2ra20508d","article-title":"Organochalcogen ligands and their palladium(II) complexes: synthesis to catalytic activity for Heck coupling","volume":"2","author":"Kumar","year":"2012","journal-title":"RSC Adv."},{"key":"10.1016\/j.jhazmat.2013.11.045_bib0285","doi-asserted-by":"crossref","first-page":"609","DOI":"10.1002\/adsc.200505473","article-title":"On the nature of the active species in palladium catalyzed Mizoroki\u2013Heck and Suzuki\u2013Miyaura couplings \u2013 homogeneous or heterogeneous catalysis, a critical review","volume":"348","author":"Phan","year":"2006","journal-title":"Adv. Synth. Catal."},{"key":"10.1016\/j.jhazmat.2013.11.045_bib0290","article-title":"Efficient catalysis of Suzuki-Miyaura C-C coupling reactions with palladium(II) complexes of partially hydrolyzed bisimine ligands: a process important in environment context","author":"Kumar","year":"2013","journal-title":"J. Hazard. Mater"}],"container-title":["Journal of Hazardous Materials"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S030438941300900X?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S030438941300900X?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2018,10,8]],"date-time":"2018-10-08T16:57:16Z","timestamp":1539017836000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S030438941300900X"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2014,3]]},"references-count":58,"alternative-id":["S030438941300900X"],"URL":"https:\/\/doi.org\/10.1016\/j.jhazmat.2013.11.045","relation":{},"ISSN":["0304-3894"],"issn-type":[{"value":"0304-3894","type":"print"}],"subject":[],"published":{"date-parts":[[2014,3]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Complex of 2-(methylthio)aniline with palladium(II) as an efficient catalyst for Suzuki\u2013Miyaura CC coupling in eco-friendly water","name":"articletitle","label":"Article Title"},{"value":"Journal of Hazardous Materials","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.jhazmat.2013.11.045","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"Copyright \u00a9 2013 Elsevier B.V. All rights reserved.","name":"copyright","label":"Copyright"}]}}