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Ma, Xiaoli
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Ma, Xiaoli
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Ma, Xiaoli
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Ma, X.
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2007Journal Article [["dc.bibliographiccitation.firstpage","7093"],["dc.bibliographiccitation.issue","17"],["dc.bibliographiccitation.journal","Inorganic Chemistry"],["dc.bibliographiccitation.lastpage","7096"],["dc.bibliographiccitation.volume","46"],["dc.contributor.author","Yang, Zhi"],["dc.contributor.author","Ma, Xiaoli"],["dc.contributor.author","Roesky, Herbert W."],["dc.contributor.author","Yang, Y."],["dc.contributor.author","Magull, Joerg"],["dc.contributor.author","Ringe, Arne"],["dc.date.accessioned","2018-11-07T10:59:34Z"],["dc.date.available","2018-11-07T10:59:34Z"],["dc.date.issued","2007"],["dc.description.abstract","A series of novel aluminum heterobimetallic selenicles were reported. The reaction of LAI(SeH)(2) (1) with LiN(SiMe(3))(2) resulted in the formation of [LAI(SeLi)(2)(THF)(2)] (2) (L = HC(CMeNAr)(2), Ar = 2,6-iPr(2)C(6)H(3))- Compound 2 reacted with Me(2)GeCl(2), Ph(2)GeCl(2), CP(2)TiCl(2), and CP(2)ZrCl(2), respectively, to produce LAI(mu-Se)(2)GeMe(2) (3), LAI(mu-Se)(2)GePh(2) (4), LAI(mu-Se)(2)TiCP(2) (5), and LAI(mu-Se)(2)ZrCp(2) (6) in moderate yields. Compounds 2-6 were characterized by elemental analysis, NMR, and electron impact-MS. The X-ray single-crystal structure of 3 is reported and confirms the spirocyclic arrangement of the aluminum atom within the six-membered AlN(2)C(3) and four-membered AlSe(2)Ge rings."],["dc.identifier.doi","10.1021/ic700945a"],["dc.identifier.isi","000248757200039"],["dc.identifier.pmid","17608418"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/50735"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Amer Chemical Soc"],["dc.relation.issn","0020-1669"],["dc.title","Synthesis and characterization of well-defined aluminum-containing heterobi metallic selenides"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]Details DOI PMID PMC WOS2013Journal Article [["dc.bibliographiccitation.firstpage","2618"],["dc.bibliographiccitation.issue","14"],["dc.bibliographiccitation.journal","Zeitschrift für anorganische und allgemeine Chemie"],["dc.bibliographiccitation.lastpage","2622"],["dc.bibliographiccitation.volume","639"],["dc.contributor.author","Yang, Zhi"],["dc.contributor.author","Hao, Pengfei"],["dc.contributor.author","Liu, Zhihong"],["dc.contributor.author","Ma, Xiaoli"],["dc.contributor.author","Roesky, Herbert W."],["dc.contributor.author","Yang, Y."],["dc.contributor.author","Li, Jiarong"],["dc.date.accessioned","2018-11-07T09:17:46Z"],["dc.date.available","2018-11-07T09:17:46Z"],["dc.date.issued","2013"],["dc.description.abstract","The reaction of LAlMe2 (1) [L = HC(CMeNAr)(2), Ar = 2, 6-iPr(2)C(6)H(3)] with diphenylstannanediol resulted in the methylalumoxane compound L(Me)Al(-O)Al(Me)L (3). Compound (LAlO)(2)B(2, 6-OCH3C6H4)(-O) (4) containing the Al2BO3 six-membered ring was accomplished by reacting the precursor LAlH2 (2) with 2, 6-dimethoxyphenylboronic acid. The two compounds were characterized by H-1 NMR spectroscopy, elemental analysis, and single-crystal X-ray structural analysis."],["dc.identifier.doi","10.1002/zaac.201300386"],["dc.identifier.isi","000329497900041"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/28249"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Wiley-v C H Verlag Gmbh"],["dc.relation.issn","1521-3749"],["dc.relation.issn","0044-2313"],["dc.title","Synthesis and Structural Characterization of Compounds Containing the Al-O-Al Motif"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]Details DOI WOS2014Journal Article [["dc.bibliographiccitation.firstpage","1081"],["dc.bibliographiccitation.issue","6"],["dc.bibliographiccitation.journal","Zeitschrift für anorganische und allgemeine Chemie"],["dc.bibliographiccitation.lastpage","1085"],["dc.bibliographiccitation.volume","640"],["dc.contributor.author","Yang, Zhi"],["dc.contributor.author","Hao, Pengfei"],["dc.contributor.author","Ma, Xiaoli"],["dc.contributor.author","Roesky, Herbert W."],["dc.contributor.author","Yang, Y."],["dc.contributor.author","Li, Jiarong"],["dc.date.accessioned","2018-11-07T09:40:38Z"],["dc.date.available","2018-11-07T09:40:38Z"],["dc.date.issued","2014"],["dc.description.abstract","The reaction of 1, 6-bis(trimethylsilylamino)benzene (LH2) (1) in toluene with H3Al center dot NMe3 yielded the aluminum monohydride with coordinate NMe3 of composition [1, 6-(Me3SiN)(2)C6H4]AlH(NMe3) (2). However, the same reaction in THF resulted in the ring opening of THF with formation of {[1, 6-(Me3SiN)(2)C6H4]AlH}(2)O(CH2)(4)NMe3 (3) in good yield. Both the spectroscopic data in solution as well as the X-ray crystallographic data confirmed that a THF molecule underwent a ring-opening reaction. Compound 2 is the first monomeric aluminum hydride compound containing the 1, 6-bis(trimethylsilylamino)benzene. Compound 3 exhibits an intermolecular zwitterion of composition O-(CH2)(4)NMe3+ between two aluminum atoms. Complexes 2 and 3 were characterized by H-1 NMR spectroscopy, elementary analysis, and single-crystal X-ray diffraction studies."],["dc.identifier.doi","10.1002/zaac.201300608"],["dc.identifier.isi","000335973100010"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/33549"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Wiley-v C H Verlag Gmbh"],["dc.relation.issn","1521-3749"],["dc.relation.issn","0044-2313"],["dc.title","Synthesis of 1,6-Bis( trimethylsilylamino) benzene- Substituted Aluminum Hydrides: The Characterization of a Product from Ring- Opening Reaction of Tetrahydrofuran"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]Details DOI WOS2015Journal Article [["dc.bibliographiccitation.firstpage","521"],["dc.bibliographiccitation.issue","3-4"],["dc.bibliographiccitation.journal","Zeitschrift für anorganische und allgemeine Chemie"],["dc.bibliographiccitation.lastpage","524"],["dc.bibliographiccitation.volume","641"],["dc.contributor.author","Ju, Yingxin"],["dc.contributor.author","Yang, Zhi"],["dc.contributor.author","Ma, Xiaoli"],["dc.contributor.author","Yang, Y."],["dc.contributor.author","Roesky, Herbert W."],["dc.date.accessioned","2018-11-07T10:00:20Z"],["dc.date.available","2018-11-07T10:00:20Z"],["dc.date.issued","2015"],["dc.description.abstract","An aluminum(III) monohydride [(2, 6-iPr(2)C(6)H(3))NC(Me)](2)AlH(NMe3) (1) was synthesized by oxidative addition of 1, 2-diimine (L) {L = [(2, 6-iPr(2)C(6)H(3))NC(Me)](2)} with equivalent amounts of H3AlNMe3. A lithium salt (LLi2) was obtained when L was treated with elemental lithium. Under these conditions 1, 2-diimine is reduced to LLi2 with simultaneous formation of a C=C bond. The LLi2 is formed in-situ and treated with AlBr3 to result in the formation of aluminum(III) monobromide [(2, 6-iPr(2)C(6)H(3))NC(Me)](2)AlBr(OEt2) (2). The two products 1 and 2 show a saturated as well as an unsaturated backbone of the ligand."],["dc.identifier.doi","10.1002/zaac.201400611"],["dc.identifier.isi","000351445600002"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/37784"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Wiley-v C H Verlag Gmbh"],["dc.relation.issn","1521-3749"],["dc.relation.issn","0044-2313"],["dc.title","A Saturated and Unsaturated Backbone of the Products from the Reaction of 1,2-Diimine with Aluminum Precursors"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]Details DOI WOS2007Journal Article [["dc.bibliographiccitation.firstpage","4919"],["dc.bibliographiccitation.issue","31"],["dc.bibliographiccitation.journal","European Journal of Inorganic Chemistry"],["dc.bibliographiccitation.lastpage","4922"],["dc.contributor.author","Yang, Zhi"],["dc.contributor.author","Ma, Xiaoli"],["dc.contributor.author","Roesky, Herbert W."],["dc.contributor.author","Yang, Y."],["dc.contributor.author","Jimenez-Perez, Victor Manuel"],["dc.contributor.author","Magull, Joerg"],["dc.contributor.author","Ringe, Arne"],["dc.contributor.author","Jones, Peter G."],["dc.date.accessioned","2018-11-07T10:56:15Z"],["dc.date.available","2018-11-07T10:56:15Z"],["dc.date.issued","2007"],["dc.description.abstract","The reaction of 1,8-bis(trimethylsilylamino)naphthalene (LH(2)) (1) with nBuLi yields the dilithium compound [1,8(Me(3)SiN)(2)C(10)H(6)](Li)(2)(thf)(3) (2). Compound 1 reacts with H(3)Al center dot NMe(3) with elimination of hydrogen gas to produce [1,8-(Me(3)SiN)(2)C(10)H(6)]AlH(NMe(3)) (3), and the reaction of 2 with MeAlCl(2) leads to [1,8-(Me(3)SiN)(2)C(10)H(6)]Al(Me)thf (4). Compounds 3 and 4 are the first two aluminum mononuclear compounds to contain the 1,8-diaminonaphthalene ligand. These compounds were characterized by elemental analysis, NMR and IR spectroscopy, MS, and single-crystal X-ray structural analysis. ((c) Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2007)."],["dc.identifier.doi","10.1002/ejic.200700477"],["dc.identifier.isi","000250940500009"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/49969"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Wiley-blackwell"],["dc.relation.issn","1434-1948"],["dc.title","Syntheses, characterizations, and X-ray single-crystal structures of 1,8-bis(trimethylsilylamino)naphthalene aluminum hydride and the methyl derivative"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]Details DOI WOS2015Journal Article [["dc.bibliographiccitation.firstpage","105"],["dc.bibliographiccitation.issue","1"],["dc.bibliographiccitation.journal","Organometallics"],["dc.bibliographiccitation.lastpage","108"],["dc.bibliographiccitation.volume","34"],["dc.contributor.author","Hao, Pengfei"],["dc.contributor.author","Yang, Zhi"],["dc.contributor.author","Li, Wenling"],["dc.contributor.author","Ma, Xiaoli"],["dc.contributor.author","Roesky, Herbert W."],["dc.contributor.author","Yang, Y."],["dc.contributor.author","Li, Jiarong"],["dc.date.accessioned","2018-11-07T10:02:16Z"],["dc.date.available","2018-11-07T10:02:16Z"],["dc.date.issued","2015"],["dc.description.abstract","Three aluminum complexes, LAl(OCH2C6H4-2-NH2)(2) (2), LAl(9-OC13H9)(2) (3), and LAl(OC6H10-4-NH2)(2) (4), were synthesized in good yield by reacting one equivalent of LAlH2 (1) (L = HC(CMeNAr)(2), Ar = 2,6-iPr(2)C(6)H(3)) with two equivalents of 2-aminobenzyl alcohol, 9-hydroxyfluorene, and trans-4-aminocyclohexanol, respectively. All complexes (2, 3, and 4) contain the COAlOC framework. These complexes have been characterized by IR, H-1 and C-13 NMR, elemental analyses, and single-crystal X-ray structural analysis. Furthermore, the excellent catalytic activities of 2, 3, and 4 for ring-opening polymerization of e-caprolactone in the presence of isopropyl alcohol were investigated."],["dc.identifier.doi","10.1021/om500950p"],["dc.identifier.isi","000347864300014"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/38191"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Amer Chemical Soc"],["dc.relation.issn","1520-6041"],["dc.relation.issn","0276-7333"],["dc.title","Aluminum Complexes Containing the C-O-Al-O-C Framework as Efficient Initiators for Ring-Opening Polymerization of epsilon-Caprolactone"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]Details DOI WOS2008Journal Article [["dc.bibliographiccitation.firstpage","1490"],["dc.bibliographiccitation.issue","9"],["dc.bibliographiccitation.journal","Zeitschrift für anorganische und allgemeine Chemie"],["dc.bibliographiccitation.lastpage","1492"],["dc.bibliographiccitation.volume","634"],["dc.contributor.author","Yang, Zhi"],["dc.contributor.author","Ma, Xiaoli"],["dc.contributor.author","Roesky, Herbert W."],["dc.contributor.author","Yang, Y."],["dc.contributor.author","Zhu, Hongping"],["dc.contributor.author","Magull, Joerg"],["dc.contributor.author","Ringe, Arne"],["dc.date.accessioned","2018-11-07T11:20:54Z"],["dc.date.available","2018-11-07T11:20:54Z"],["dc.date.issued","2008"],["dc.description.abstract","The germanium(II) and gallium(III) organochlorides containing the C(6)F(5)-substituted beta-diketiminate ligand LGeCl (2) and LGaCl(2) (3) (L = HC[(CMe)(NC(6)F(5))](2)) were synthesized. Salt elimination reactions of the C6F5-substituted beta-diketiminato lithium salt with the corresponding germanium(II) and gallium(III) chlorides led to the organochlorides respectively. Compounds 2 and 3 were characterized by spectroscopic and elemental analyses, and 2 was further investigated by single crystal X-ray structural analysis."],["dc.identifier.doi","10.1002/zaac.200800087"],["dc.identifier.isi","000258459500007"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/55646"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Wiley-blackwell"],["dc.relation.issn","0044-2313"],["dc.title","Synthesis and characterization of gallium(M) and germanium(H) chlorides bearing the C(6)F(5)-substituted beta-diketiminate HC[(CMe)(NC(6)F(5))](2) ligand"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]Details DOI WOS