Samuel, Prinson Poikayil

[["dc.bibliographiccitation.firstpage","19041"],["dc.bibliographiccitation.issue","52"],["dc.bibliographiccitation.journal","Chemistry - A European Journal"],["dc.bibliographiccitation.lastpage","19047"],["dc.bibliographiccitation.volume","21"],["dc.contributor.author","Sarish, Sankaranarayana Pillai"],["dc.contributor.author","Samuel, Prinson P."],["dc.contributor.author","Roesky, Herbert W."],["dc.contributor.author","Schulzke, Carola"],["dc.contributor.author","Nijesh, Karikkeeriyil"],["dc.contributor.author","De, Susmita"],["dc.contributor.author","Parameswaran, Pattiyil"],["dc.date.accessioned","2018-11-07T09:47:23Z"],["dc.date.available","2018-11-07T09:47:23Z"],["dc.date.issued","2015"],["dc.description.abstract","A beta-diketiminate Al compound (1) with an exocyclic double bond reacts with two equivalents each of benzophenone and 2-benzoylpyridine in a [4+2] cycloaddition to generate bicyclic and tricyclic compounds 2 and 3, respectively. Compound 2 consists of six-and eight-membered aluminium rings, whereas 3 has two five-and one eight-membered ring. Compounds 2 and 3 were characterized by a number of analytical tools including single-crystal X-ray diffraction. The quantum mechanical calculations suggest that the dissociation of the solvent molecule from 1 would lead to an active species 1A having two 1,4-dipolar 4 pi electron moieties, in which the electrophilic site is the Al atom and the nucleophilic positions are polarized exocyclic and endocyclic C=C pi bonds. The detailed mechanistic study shows that the dipolarophiles, benzophenone, and 2-benzoylpyridine undergo double cycloaddition with two 1,4-dipolar 4 pi electron moieties of 1A. Herein, the addition of one molecule of the dipolarophile promotes the addition of the second one."],["dc.identifier.doi","10.1002/chem.201503137"],["dc.identifier.isi","000368282100025"],["dc.identifier.pmid","26593152"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/35104"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Wiley-v C H Verlag Gmbh"],["dc.relation.issn","1521-3765"],["dc.relation.issn","0947-6539"],["dc.title","Multiple Cycloaddition Reactions of Ketones with a beta-Diketiminate Al Compound"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","354"],["dc.bibliographiccitation.issue","1"],["dc.bibliographiccitation.journal","Organometallics"],["dc.bibliographiccitation.lastpage","357"],["dc.bibliographiccitation.volume","32"],["dc.contributor.author","Singh, Amit Pratap"],["dc.contributor.author","Samuel, Prinson P."],["dc.contributor.author","Mondal, Kartik Chandra"],["dc.contributor.author","Roesky, Herbert W."],["dc.contributor.author","Sidhu, Navdeep S."],["dc.contributor.author","Dittrich, Birger"],["dc.date.accessioned","2018-11-07T09:29:12Z"],["dc.date.available","2018-11-07T09:29:12Z"],["dc.date.issued","2013"],["dc.description.abstract","The chemistry of stable metalylenes (the heavier group 14 element analogues of carbenes) is an intriguing target of main group chemistry due to their synthetic potential and industrial application. In the present study, we report on the utilization of an abnormal N-heterocyclic carbene (aNHC) and a cyclic alkylamino carbene (cAAC) as a Lewis base for the syntheses of compounds aNHC-SiCl2 (3), aNHC-SnCl2 (4), and cAAC.SnCl2 (5). The synthesis of silylene 3 involved the ligand-substitution reaction between NHC-SiCl2 and an aNHC. However, compounds 4 and 5 were synthesized by the reactions of aNHC and cAAC with SnCl2 in the molar ratio of 1:1. Compounds 3-5 are well-characterized with various spectroscopic methods and single-crystal X-ray structural analysis."],["dc.description.sponsorship","Deutsche Forschungsgemeinschaft"],["dc.identifier.doi","10.1021/om301062d"],["dc.identifier.isi","000313606200041"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/30964"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Amer Chemical Soc"],["dc.relation.issn","0276-7333"],["dc.title","Lewis Base Stabilized Group 14 Metalylenes"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","7324"],["dc.bibliographiccitation.issue","19"],["dc.bibliographiccitation.journal","Journal of the American Chemical Society"],["dc.bibliographiccitation.lastpage","7329"],["dc.bibliographiccitation.volume","135"],["dc.contributor.author","Singh, Amit Pratap"],["dc.contributor.author","Samuel, Prinson P."],["dc.contributor.author","Roesky, Herbert W."],["dc.contributor.author","Schwarzer, Martin C."],["dc.contributor.author","Frenking, Gernot"],["dc.contributor.author","Sidhu, Navdeep S."],["dc.contributor.author","Dittrich, Birger"],["dc.date.accessioned","2018-11-07T09:24:41Z"],["dc.date.available","2018-11-07T09:24:41Z"],["dc.date.issued","2013"],["dc.description.abstract","Metal ions with radical centers in their coordination sphere are key participants in biological and catalytic processes. In the present study, we describe the synthesis of the cAAC:ZnCl2 adduct (1) using a cyclic alkylaminocarbene (cAAC) as donor ligand. Compound 1 was treated with 2 equiv of KC8 and LiB(sec-Bu)(3)H to yield a deep blue-colored dicarbene zinc compound (cAAC)(2)Zn (2) and the colorless hydrogenated zinc compound (cAACH)(2)Zn (3), respectively. Compounds 2 and 3 were well characterized by spectroscopic methods and single-crystal X-ray structural analysis. Density functional theory calculations were performed for 2 which indicate that this molecule possesses a singlet biradicaloid character. Moreover, we show the application of 2 in CO2 activation, which yields a zwitterionic cAAC center dot CO2 adduct."],["dc.description.sponsorship","Deutsche Forschungsgemeinschaft (DFG) [RO 224/60-1]"],["dc.identifier.doi","10.1021/ja402351x"],["dc.identifier.isi","000319250200035"],["dc.identifier.pmid","23600486"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/29883"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Amer Chemical Soc"],["dc.relation.issn","0002-7863"],["dc.title","A Singlet Biradicaloid Zinc Compound and Its Nonradical Counterpart"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","12940"],["dc.bibliographiccitation.issue","36"],["dc.bibliographiccitation.journal","Dalton Transactions"],["dc.bibliographiccitation.lastpage","12946"],["dc.bibliographiccitation.volume","42"],["dc.contributor.author","Tretiakov, Mykyta"],["dc.contributor.author","Shermolovich, Yuriy G."],["dc.contributor.author","Singh, Amit Pratap"],["dc.contributor.author","Samuel, Prinson P."],["dc.contributor.author","Roesky, Herbert W."],["dc.contributor.author","Niepoetter, Benedikt"],["dc.contributor.author","Visscher, Arne"],["dc.contributor.author","Stalke, Dietmar"],["dc.date.accessioned","2018-11-07T09:29:43Z"],["dc.date.available","2018-11-07T09:29:43Z"],["dc.date.issued","2013"],["dc.description.abstract","Oxidation reactions of stable chalcogenamides with iodine are intriguing due to their broad application in various organic syntheses. In the present study we report on the utilization of N-heterocyclic carbene and cyclic-alkyl-amino carbenes L1-3: (L-1: = :C[N(2,6-Pr-i(2)-C6H3)CH](2), L-2: = :C(CH2)(CMe2)(C6H10)N-2,6-Pr-i(2)-C6H3, L-3: = :C(CH2)(CMe2)(2)N-2,6-Pr-i(2)-C6H3) for the syntheses of chalcogenamides L1-3=E (E = S, Se, Te) 1-4 and zwitterionic adducts L1-3=E-I-I 5-8. The synthesis of compounds 1-4 involved the addition reaction of ligand L1-3: and elemental chalcogen. Treatment of 1-4 with iodine resulted in the formation of adducts 5-8. Compounds 5-8 are well characterized with various spectroscopic methods and single-crystal X-ray structural analysis."],["dc.description.sponsorship","Deutsche Forschungsgemeinschaft"],["dc.identifier.doi","10.1039/c3dt51309b"],["dc.identifier.isi","000323274800024"],["dc.identifier.pmid","23770833"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/10780"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/31110"],["dc.notes.intern","Merged from goescholar"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Royal Soc Chemistry"],["dc.relation.issn","1477-9226"],["dc.rights","Goescholar"],["dc.rights.uri","https://goescholar.uni-goettingen.de/licenses"],["dc.title","Lewis-base stabilized diiodine adducts with N-heterocyclic chalcogenamides"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","192"],["dc.bibliographiccitation.issue","1"],["dc.bibliographiccitation.journal","Chemical Communications"],["dc.bibliographiccitation.lastpage","195"],["dc.bibliographiccitation.volume","53"],["dc.contributor.author","Kundu, Subrata"],["dc.contributor.author","Mohapatra, Chandrajeet"],["dc.contributor.author","Samuel, Prinson P."],["dc.contributor.author","Kretsch, Johannes"],["dc.contributor.author","Walawalkar, M. G."],["dc.contributor.author","Herbst-Irmer, Regine"],["dc.contributor.author","Stalke, Dietmar"],["dc.contributor.author","De, Sriman"],["dc.contributor.author","Koley, Debasis"],["dc.contributor.author","Roesky, Herbert W."],["dc.date.accessioned","2021-06-01T10:50:46Z"],["dc.date.available","2021-06-01T10:50:46Z"],["dc.date.issued","2017"],["dc.description.abstract","The synthesis of a 1,4-bisphosphino-2,3-disila butadiene and a 1,3-diphospha-2-silaallyl anion has been reported."],["dc.description.abstract","The first acyclic 4π-electron –PSi–SiP– motif with two four coordinate silicon substituents supported by the amidinate ligand and two coordinate phosphorus has been synthesized from the reaction of heteroleptic chlorosilylene LSiCl (1), TripPCl 2 (Trip = 2,4,6- i Pr 3 C 6 H 2 ) and KC 8 in a 1 : 1 : 3 ratio. The same reaction in a 1 : 2 : 6 ratio in the presence of one equivalent of 18-crown-6 ether affords the 1,3-diphospha-2-silaallyl anion."],["dc.identifier.doi","10.1039/C6CC09171G"],["dc.identifier.eissn","1364-548X"],["dc.identifier.issn","1359-7345"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/13973"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/86779"],["dc.language.iso","en"],["dc.notes.intern","DOI-Import GROB-425"],["dc.relation.eissn","1364-548X"],["dc.relation.issn","1359-7345"],["dc.rights.access","openAccess"],["dc.title","An unprecedented 1,4-diphospha-2,3-disila butadiene (–PSi–SiP–) derivative and a 1,3-diphospha-2-silaallyl anion, each stabilized by the amidinate ligand"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","10530"],["dc.bibliographiccitation.issue","34"],["dc.bibliographiccitation.journal","Chemistry - A European Journal"],["dc.bibliographiccitation.lastpage","10545"],["dc.bibliographiccitation.volume","18"],["dc.contributor.author","Mukherjee, Arup"],["dc.contributor.author","Sen, Tamal K."],["dc.contributor.author","Ghorai, Pradip Kr."],["dc.contributor.author","Samuel, Prinson P."],["dc.contributor.author","Schulzke, Carola"],["dc.contributor.author","Mandal, Swadhin K."],["dc.date.accessioned","2018-11-07T09:07:36Z"],["dc.date.available","2018-11-07T09:07:36Z"],["dc.date.issued","2012"],["dc.description.abstract","Herein, we report the synthesis and characterization of two organozinc complexes that contain symmetrical phenalenyl (PLY)-based N,N-ligands. The reactions of phenalenyl-based ligands with ZnMe2 led to the formation of organozinc complexes [N(Me),N(Me)-PLY]ZnMe (1) and [N(iPr),N(iPr)-PLY]ZnMe (2) under the evolution of methane. Both complexes (1 and 2) were characterized by NMR spectroscopy and elemental analysis. The solid-state structures of complexes 1 and 2 were determined by single-crystal X-ray crystallography. Complexes 1 and 2 were used as catalysts for the intramolecular hydroamination of unactivated primary and secondary aminoalkenes. A combined approach of NMR spectroscopy and DFT calculations was utilized to obtain better insight into the mechanistic features of the zinc-catalyzed hydroamination reactions. The progress of the catalysis for primary and secondary aminoalkene substrates with catalyst 2 was investigated by detailed kinetic studies, including kinetic isotope effect measurements. These results suggested pseudo-first-order kinetics for both primary and secondary aminoalkene activation processes. Eyring and Arrhenius analyses for the cyclization of a model secondary aminoalkene substrate afforded ?H?=11.3 kcal?mol-1, ?S?=-35.75 cal?K-1?mol-1, and Ea=11.68 kcal?mol-1. Complex 2 exhibited much-higher catalytic activity than complex 1 under identical reaction conditions. The in situ NMR experiments supported the formation of a catalytically active zinc cation and the DFT calculations showed that more active catalyst 2 generated a more stable cation. The stability of the catalytically active zinc cation was further supported by an in situ recycling procedure, thereby confirming the retention of catalytic activity of compound 2 for successive catalytic cycles. The DFT calculations showed that the preferred pathway for the zinc-catalyzed hydroamination reactions is alkene activation rather than the alternative amine-activation pathway. A detailed investigation with DFT methods emphasized that the remarkably higher catalytic efficiency of catalyst 2 originated from its superior stability and the facile formation of its cation compared to that derived from catalyst 1."],["dc.description.sponsorship","IISER-Kolkata; CSIR, India [01(2369)/10/EMR-II]; DST, India"],["dc.identifier.doi","10.1002/chem.201200868"],["dc.identifier.isi","000307387300012"],["dc.identifier.pmid","22807308"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/25834"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Wiley-v C H Verlag Gmbh"],["dc.relation.issn","0947-6539"],["dc.title","Phenalenyl-Based Organozinc Catalysts for Intramolecular Hydroamination Reactions: A Combined Catalytic, Kinetic, and Mechanistic Investigation of the Catalytic Cycle"],["dc.type","review"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","12572"],["dc.bibliographiccitation.issue","36"],["dc.bibliographiccitation.journal","Chemistry - A European Journal"],["dc.bibliographiccitation.lastpage","+"],["dc.bibliographiccitation.volume","21"],["dc.contributor.author","Mohapatra, Chandrajeet"],["dc.contributor.author","Mondal, Kartik Chandra"],["dc.contributor.author","Samuel, Prinson P."],["dc.contributor.author","Keil, Helena"],["dc.contributor.author","Niepoetter, Benedikt"],["dc.contributor.author","Herbst-Irmer, Regine"],["dc.contributor.author","Stalke, Dietmar"],["dc.contributor.author","Dutta, Sayan"],["dc.contributor.author","Koley, Debasis"],["dc.contributor.author","Roesky, Herbert W."],["dc.date.accessioned","2018-11-07T09:52:44Z"],["dc.date.available","2018-11-07T09:52:44Z"],["dc.date.issued","2015"],["dc.description.abstract","The Me-cAAC:-stabilized dimer of silicon disulfide (SiS2) has been isolated in the molecular form as (Me-cAAC:)(2)Si2S4 (2) at room temperature [Me-cAAC:=cyclic alkyl(amino) carbene]. Compound 2 has been synthesized from the reaction of (Me-cAAC:)(2)Si-2 with elemental sulfur in a 1:4 molar ratio under oxidative addition. This is the smallest molecular unit of silicon disulfide characterized by X-ray crystallography, electron ionization mass spectrometry, and NMR spectroscopy. Structures with three sulfur atoms arranged around a silicon atom are known; however, 2 is the first structurally characterized silicon-sulfur compound containing one terminal and two bridging sulfur atoms at each silicon atom. Compound 2 shows no decomposition after storing for three months in an inert atmosphere at ambient temperature. The bonding of 2 has been further studied by theoretical calculations."],["dc.identifier.doi","10.1002/chem.201502092"],["dc.identifier.isi","000360312100001"],["dc.identifier.pmid","26179976"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/36187"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Wiley-v C H Verlag Gmbh"],["dc.relation.issn","1521-3765"],["dc.relation.issn","0947-6539"],["dc.title","A Stable Dimer of SiS2 Arranged between Two Carbene Molecules"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","1953"],["dc.bibliographiccitation.issue","5"],["dc.bibliographiccitation.journal","Inorganic Chemistry"],["dc.bibliographiccitation.lastpage","1955"],["dc.bibliographiccitation.volume","55"],["dc.contributor.author","Mohapatra, Chandrajeet"],["dc.contributor.author","Samuel, Prinson P."],["dc.contributor.author","Li, Bin"],["dc.contributor.author","Niepoetter, Benedikt"],["dc.contributor.author","Schuermann, Christian J."],["dc.contributor.author","Herbst-Irmer, Regine"],["dc.contributor.author","Stalke, Dietmar"],["dc.contributor.author","Maity, Bholanath"],["dc.contributor.author","Koley, Debasis"],["dc.contributor.author","Roesky, Herbert W."],["dc.date.accessioned","2018-11-07T10:16:56Z"],["dc.date.available","2018-11-07T10:16:56Z"],["dc.date.issued","2016"],["dc.description.abstract","Carbenes are known for their ability to abstract HCl from hydrochlorosilanes to form carbene hydrochloride adducts. In contrast, the Si-H bond insertion products RSiCl2(cAACH) (2, 4, 6, and 8) have been formed in the reaction of RSiHCl2 [R = Ar(SiMe3)N (1), Cp (3), PhC(NtBu)(2) (5), Cl (7); Ar = 2,6-iPr(2)C(6)H(3)] with a cyclic alkyl(amino) carbene (cAAC:) irrespective of the steric demand of the R group. The new products have been characterized by various analytical tools including X-ray crystallography, electron ionization mass spectrometry, and NMR spectroscopy. Theoretical investigations have also been performed to understand why cAAC prefers insertion into the Si-H bond rather than the dehydrohalogenation pathway."],["dc.identifier.doi","10.1021/acs.inorgchem.6b00024"],["dc.identifier.isi","000371753500001"],["dc.identifier.pmid","26859316"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/41136"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Amer Chemical Soc"],["dc.relation.issn","1520-510X"],["dc.relation.issn","0020-1669"],["dc.title","Insertion of Cyclic Alkyl(amino) Carbene into the Si-H Bonds of Hydrochlorosilanes"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","1544"],["dc.bibliographiccitation.issue","3"],["dc.bibliographiccitation.journal","Inorganic Chemistry"],["dc.bibliographiccitation.lastpage","1549"],["dc.bibliographiccitation.volume","52"],["dc.contributor.author","Samuel, Prinson P."],["dc.contributor.author","Singh, Amit Pratap"],["dc.contributor.author","Sarish, Sankaranarayana Pillai"],["dc.contributor.author","Matussek, Julia"],["dc.contributor.author","Objartel, Ina"],["dc.contributor.author","Roesky, Herbert W."],["dc.contributor.author","Stalke, Dietmar"],["dc.date.accessioned","2018-11-07T09:28:16Z"],["dc.date.available","2018-11-07T09:28:16Z"],["dc.date.issued","2013"],["dc.description.abstract","Diallcylamino compounds of group 14 elements (Si, Ge, Sn) in the +2 oxidation state supported by benzamidinate ligands were synthesized and treated with pentafluoropyridine. Two different modes of reactivity were observed, depending on the metal atom and the basicity of the substituent at the metal. Pentafluoropyridine undergoes oxidative addition reaction at the Si(II) and Ge(II) atoms whereas at the Sn(II) atom substitution of the NMe2 group by the para fluorine of pentafluoropyridine occurs. The C F bond activation by the lone pair of germanium is the first report of this kind. The Sn(II) fluoride obtained has an elongated Sn F bond length and can be used as a good fluorinating agent. The compounds were characterized by multinuclear NMR spectroscopy, mass spectrometry, elemental analysis, and X-ray structural analysis. Single crystal X-ray structural analysis of the tin fluoride shows an asymmetric dimer with weak Sn(II)(F) (F)Sn(II) interactions."],["dc.description.sponsorship","Center for Materials Crystallography (CMC); Land Niedersachsen"],["dc.identifier.doi","10.1021/ic302344a"],["dc.identifier.isi","000314627700044"],["dc.identifier.pmid","23343458"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/30733"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Amer Chemical Soc"],["dc.relation.issn","0020-1669"],["dc.title","Oxidative Addition Versus Substitution Reactions of Group 14 Dialkylamino Metalylenes with Pentafluoropyridine"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","11817"],["dc.bibliographiccitation.issue","45"],["dc.bibliographiccitation.journal","Angewandte Chemie International Edition"],["dc.bibliographiccitation.lastpage","11821"],["dc.bibliographiccitation.volume","52"],["dc.contributor.author","Samuel, Prinson P."],["dc.contributor.author","Mondal, Kartik Chandra"],["dc.contributor.author","Roesky, Herbert W."],["dc.contributor.author","Hermann, Markus"],["dc.contributor.author","Frenking, Gernot"],["dc.contributor.author","Demeshko, Serhiy"],["dc.contributor.author","Meyer, Franc"],["dc.contributor.author","Stueckl, A. Claudia"],["dc.contributor.author","Christian, Jonathan H."],["dc.contributor.author","Dalal, Naresh S."],["dc.contributor.author","Ungur, Liviu"],["dc.contributor.author","Chibotaru, Liviu F."],["dc.contributor.author","Proepper, Kevin"],["dc.contributor.author","Meents, Alke"],["dc.contributor.author","Dittrich, Birger"],["dc.date.accessioned","2018-11-07T09:17:42Z"],["dc.date.available","2018-11-07T09:17:42Z"],["dc.date.issued","2013"],["dc.description.sponsorship","Deutsche Forschungsgemeinschaft [RO 224/60-1]"],["dc.identifier.doi","10.1002/anie.201304642"],["dc.identifier.isi","000326138500029"],["dc.identifier.pmid","24038991"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/28227"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Wiley-v C H Verlag Gmbh"],["dc.relation.issn","1521-3773"],["dc.relation.issn","1433-7851"],["dc.title","Synthesis and Characterization of a Two-Coordinate Manganese Complex and its Reaction with Molecular Hydrogen at Room Temperature"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]