Ma, Xiaoli

[["dc.bibliographiccitation.firstpage","198"],["dc.bibliographiccitation.issue","2"],["dc.bibliographiccitation.journal","Zeitschrift für anorganische und allgemeine Chemie"],["dc.bibliographiccitation.lastpage","202"],["dc.bibliographiccitation.volume","643"],["dc.contributor.author","Ma, Xiaoli"],["dc.contributor.author","Yao, Miaomiao"],["dc.contributor.author","Zhong, M."],["dc.contributor.author","Deng, Ziyan"],["dc.contributor.author","Li, Wenling"],["dc.contributor.author","Yang, Zhi"],["dc.contributor.author","Roesky, Herbert W."],["dc.date.accessioned","2018-11-07T10:28:58Z"],["dc.date.available","2018-11-07T10:28:58Z"],["dc.date.issued","2017"],["dc.description.abstract","Four aluminum alkyl compounds, [CH{(CH3)CN-2,4,6-MeC6H2}(2)AlMe2] (1), [CH{(CH3)CN-2,4,6-MeC6H2}(2)AlEt2] (2), [CH{(CH3)CN-2-iPrC(6)H(4)}(2)AlMe2] (3), and [CH{(CH3)CN-2-iPrC(6)H(4)}(2)AlEt2] (4), bearing -diketiminate ligands [CH{(Me)CN-2,4,6-MeC6H2}](2) ((LH)-H-1) and [CH{(Me)CN-2-(PrC6H4)-Pr-i}](2) ((LH)-H-2) were obtained from the reactions of trimethylaluminum, triethylaluminum with the corresponding -diketiminate, respectively. All compounds were characterized by H-1 NMR and C-13 NMR spectroscopy, single-crystal X-ray structural analysis, and elemental analysis. Compounds 1-4 were found to catalyze the ring-opening polymerization (ROP) of epsilon-caprolactone (epsilon-CL) with good activity."],["dc.identifier.doi","10.1002/zaac.201600396"],["dc.identifier.isi","000394605800012"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/43543"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","PUB_WoS_Import"],["dc.publisher","Wiley-v C H Verlag Gmbh"],["dc.relation.issn","1521-3749"],["dc.relation.issn","0044-2313"],["dc.title","Synthesis and Characterization of -Diketiminate Aluminum Compounds and Their Use in the 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"]]

[["dc.bibliographiccitation.firstpage","11918"],["dc.bibliographiccitation.issue","51"],["dc.bibliographiccitation.journal","Chemistry – A European Journal"],["dc.bibliographiccitation.lastpage","11923"],["dc.bibliographiccitation.volume","25"],["dc.contributor.author","Shen, Qiumiao"],["dc.contributor.author","Ma, Xiaoli"],["dc.contributor.author","Li, Wenling"],["dc.contributor.author","Liu, Wenqing"],["dc.contributor.author","Ding, Yi"],["dc.contributor.author","Yang, Zhi"],["dc.contributor.author","Roesky, Herbert W."],["dc.date.accessioned","2020-12-10T14:05:54Z"],["dc.date.available","2020-12-10T14:05:54Z"],["dc.date.issued","2019"],["dc.description.abstract","he effectivecatalytic activity of organoaluminumcompoundsfor the monohydroboration of carbodiimideshas beendemonstrated. Twoaluminumcomplexes,2and3,weresynthesizedandcharacterized.Theefficientcatalyticperformances of fouraluminum hydridecomplexes L1AlH2(L1=HC(CMeNAr)2,Ar=2,6-Et2C6H3;1), L2AlH2(NMe3)(L2=o-C6H4F(CH=N-Ar),Ar=2,6-Et2C6H3;2), L3AlH(L3=2,6-bis(1-methylethyl)-N-(2-pyridinylmethylene)phenylamine;3), andL4AlH(NMe3)(L4=o-C6H4(N-Dipp)(CH=N-Dipp),Dipp=2,6-iPr2C6H3;4), andan aluminum alkylcomplex L1AlMe2(5)wereusedfor the monohydroboration of carbodiimidesin-vestigatedundersolvent-free andmildconditions. Com-pounds1–3and5can produce monohydroboratedN-boryl-formamidine, whereas4can affordtheC-borylformamidineproduct. Asuggested mechanismof this reactionwas ex-plored, andthe aluminumformamidinate compound6wascharacterized by single-crystal X-ray,also astoichiometricre-actionwas investigated."],["dc.description.sponsorship","National Natural Science Foundation of China http://dx.doi.org/10.13039/501100001809"],["dc.description.sponsorship","Deutsche Forschungsgemeinschaft http://dx.doi.org/10.13039/100004807"],["dc.identifier.doi","10.1002/chem.201902000"],["dc.identifier.eissn","1521-3765"],["dc.identifier.issn","0947-6539"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/16653"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/69699"],["dc.language.iso","en"],["dc.notes.intern","DOI Import GROB-354"],["dc.relation.eissn","1521-3765"],["dc.relation.issn","1521-3765"],["dc.relation.issn","0947-6539"],["dc.relation.orgunit","Fakultät für Chemie"],["dc.rights","CC BY 4.0"],["dc.rights.access","openAccess"],["dc.rights.uri","https://creativecommons.org/licenses/by/4.0"],["dc.subject","carbodiimide; catalysts; hydroboration; organoaluminum"],["dc.subject.ddc","540"],["dc.title","Organoaluminum Compounds as Catalysts for Monohydroboration of Carbodiimides"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","14"],["dc.bibliographiccitation.journal","Coordination Chemistry Reviews"],["dc.bibliographiccitation.lastpage","29"],["dc.bibliographiccitation.volume","350"],["dc.contributor.author","Li, Wenling"],["dc.contributor.author","Ma, Xiaoli"],["dc.contributor.author","Walawalkar, Mrinalini G."],["dc.contributor.author","Yang, Zhi"],["dc.contributor.author","Roesky, Herbert W."],["dc.date.accessioned","2020-12-10T14:22:57Z"],["dc.date.available","2020-12-10T14:22:57Z"],["dc.date.issued","2017"],["dc.identifier.doi","10.1016/j.ccr.2017.03.017"],["dc.identifier.issn","0010-8545"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/71786"],["dc.language.iso","en"],["dc.notes.intern","DOI Import GROB-354"],["dc.title","Soluble aluminum hydrides function as catalysts in deprotonation, insertion, and activation reactions"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]

[["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"]]