Otte, Matthias

[["dc.bibliographiccitation.artnumber","anie.202206120"],["dc.bibliographiccitation.journal","Angewandte Chemie International Edition"],["dc.contributor.author","Bete, Sarah C."],["dc.contributor.author","May, Leander K."],["dc.contributor.author","Woite, Philipp"],["dc.contributor.author","Roemelt, Michael"],["dc.contributor.author","Otte, Matthias"],["dc.date.accessioned","2022-07-01T07:35:44Z"],["dc.date.available","2022-07-01T07:35:44Z"],["dc.date.issued","2022"],["dc.identifier.doi","10.1002/anie.202206120"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/112250"],["dc.language.iso","en"],["dc.notes.intern","DOI-Import GROB-581"],["dc.relation.eissn","1521-3773"],["dc.relation.issn","1433-7851"],["dc.rights.uri","http://onlinelibrary.wiley.com/termsAndConditions#vor"],["dc.title","A Copper Cage‐Complex as Mimic of the pMMO CuC Site"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","3462"],["dc.bibliographiccitation.issue","21"],["dc.bibliographiccitation.journal","European Journal of Inorganic Chemistry"],["dc.bibliographiccitation.lastpage","3466"],["dc.bibliographiccitation.volume","2015"],["dc.contributor.author","Spannring, Peter"],["dc.contributor.author","Yazerski, Vital A."],["dc.contributor.author","Chen, Jianming"],["dc.contributor.author","Otte, Matthias"],["dc.contributor.author","Weckhuysen, Bert M."],["dc.contributor.author","Bruijnincx, Pieter C. A."],["dc.contributor.author","Klein Gebbink, Robertus J. M."],["dc.date.accessioned","2021-04-29T10:11:11Z"],["dc.date.available","2021-04-29T10:11:11Z"],["dc.date.issued","2015"],["dc.identifier.doi","10.1002/ejic.201500213"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/84570"],["dc.relation.issn","1434-1948"],["dc.title","Regioselective Cleavage of Electron-Rich Double Bonds in Dienes to Carbonyl Compounds with [Fe(OTf)2(mix-BPBP)] and a Combination of H2O2and NaIO4"],["dc.type","journal_article"],["dc.type.internalPublication","no"],["dc.type.subtype","original_ja"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","4755"],["dc.bibliographiccitation.issue","20"],["dc.bibliographiccitation.journal","ChemCatChem"],["dc.bibliographiccitation.lastpage","4760"],["dc.bibliographiccitation.volume","10"],["dc.contributor.author","Li, Jing"],["dc.contributor.author","Lutz, Martin"],["dc.contributor.author","Otte, Matthias"],["dc.contributor.author","Klein Gebbink, Robertus J. M."],["dc.date.accessioned","2021-04-29T10:11:39Z"],["dc.date.available","2021-04-29T10:11:39Z"],["dc.date.issued","2018-10-23"],["dc.description.abstract","Trioxo-rhenium complexes are well known catalysts for the deoxydehydration (DODH) of vicinal diols (glycols). In this work, we report on the DODH of diols and biomass-derived polyols using CpttReO3 as a new catalyst (Cptt=1,3-di-tert-butylcyclopentadienyl). The DODH reaction was optimized using 2 mol % of CpttReO3 and 3-octanol as both reductant and solvent. The CpttReO3 catalyst exhibits an excellent activity for biomass-derived polyols. Specifically, glycerol is almost quantitatively converted to allyl alcohol and mucic acid gives 75 % of muconates at 91 % conversion. In addition, the loading of CpttReO3 can be reduced to 0.1 mol % to achieve a turn-over number as high as 900 per Re when using glycerol as substrate. Examination of DODH reaction profiles by NMR spectroscopy indicates that catalysis is related to Cp-ligand release, which raises questions on the nature of the actual catalyst."],["dc.identifier.doi","10.1002/cctc.201801151"],["dc.identifier.pmid","31007775"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/84577"],["dc.language.iso","en"],["dc.relation.issn","1867-3880"],["dc.title","A Cptt-Based Trioxo-Rhenium Catalyst for the Deoxydehydration of Diols and Polyols"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.subtype","original_ja"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","4427"],["dc.bibliographiccitation.issue","30"],["dc.bibliographiccitation.journal","Chemical Communications"],["dc.bibliographiccitation.lastpage","4430"],["dc.bibliographiccitation.volume","55"],["dc.contributor.author","Bete, Sarah C."],["dc.contributor.author","Würtele, Christian"],["dc.contributor.author","Otte, Matthias"],["dc.date.accessioned","2021-06-01T10:50:51Z"],["dc.date.available","2021-06-01T10:50:51Z"],["dc.date.issued","2019"],["dc.description.abstract","An imidazole-functionalised cage is synthesised that can coordinate to Cu( i ). X-ray analysis reveals a T-shaped coordination of copper by the imidazole ligands reminiscent of the coordination geometry found in enzymatic active sites. This cage complex can catalyse the oxidation of benzylic alcohols to benzaldehydes utilizing oxygen as the terminal oxidant."],["dc.identifier.doi","10.1039/C9CC00437H"],["dc.identifier.eissn","1364-548X"],["dc.identifier.issn","1359-7345"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/16218"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/86807"],["dc.language.iso","en"],["dc.notes.intern","DOI-Import GROB-425"],["dc.notes.intern","Merged from goescholar"],["dc.relation.eissn","1364-548X"],["dc.relation.issn","1359-7345"],["dc.rights","CC BY 3.0"],["dc.rights.uri","https://creativecommons.org/licenses/by/3.0"],["dc.title","A bio-inspired imidazole-functionalised copper cage complex"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","1319"],["dc.bibliographiccitation.issue","9"],["dc.bibliographiccitation.journal","European Journal of Inorganic Chemistry"],["dc.bibliographiccitation.lastpage","1332"],["dc.bibliographiccitation.volume","2016"],["dc.contributor.author","Folkertsma, Emma"],["dc.contributor.author","de Waard, Esther F."],["dc.contributor.author","Korpershoek, Gerda"],["dc.contributor.author","van Schaik, Arnoldus J."],["dc.contributor.author","Solozabal Mirón, Naiara"],["dc.contributor.author","Borrmann, Mandy"],["dc.contributor.author","Nijsse, Sjoerd"],["dc.contributor.author","Moelands, Marcel A. H."],["dc.contributor.author","Lutz, Martin"],["dc.contributor.author","Otte, Matthias"],["dc.contributor.author","Moret, Marc-Etienne"],["dc.contributor.author","Klein Gebbink, Robertus J. M."],["dc.date.accessioned","2021-04-29T10:11:19Z"],["dc.date.available","2021-04-29T10:11:19Z"],["dc.date.issued","2016"],["dc.identifier.doi","10.1002/ejic.201501406"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/84572"],["dc.relation.issn","1434-1948"],["dc.title","Mimicry of the 2-His-1-Carboxylate Facial Triad Using Bulky N,N,O-Ligands: Non-Heme Iron Complexes Featuring a Single Facial Ligand and Easily Exchangeable Co-Ligands"],["dc.type","journal_article"],["dc.type.internalPublication","no"],["dc.type.subtype","original_ja"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","93"],["dc.bibliographiccitation.journal","Topics in Current Chemistry"],["dc.bibliographiccitation.lastpage","120"],["dc.bibliographiccitation.volume","320"],["dc.contributor.author","Gansäuer, Andreas"],["dc.contributor.author","Shi, Lei"],["dc.contributor.author","Otte, Matthias"],["dc.contributor.author","Huth, Inga"],["dc.contributor.author","Rosales, Antonio"],["dc.contributor.author","Sancho-Sanz, Iris"],["dc.contributor.author","Padial, Natalia M."],["dc.contributor.author","Oltra, J. Enrique"],["dc.date.accessioned","2021-04-29T10:10:56Z"],["dc.date.available","2021-04-29T10:10:56Z"],["dc.date.issued","2012"],["dc.description.abstract","This review highlights recent developments in the field of hydrogen atom transfer (HAT) reagents that circumvent the disadvantages of classical group 14 reagents, such as Bu₃SnH. Special emphasis is laid on the lowering of bond dissociation energies (BDEs) of molecules that could, as yet, not be used as HAT reagents and on the use of organometallic HAT reagents."],["dc.identifier.doi","10.1007/128_2011_124"],["dc.identifier.pmid","21452081"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/84566"],["dc.language.iso","en"],["dc.relation.issn","0340-1022"],["dc.title","Hydrogen atom donors: recent developments"],["dc.type","journal_article"],["dc.type.internalPublication","no"],["dc.type.subtype","original_ja"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","3106"],["dc.bibliographiccitation.issue","5"],["dc.bibliographiccitation.journal","ACS Catalysis"],["dc.bibliographiccitation.lastpage","3112"],["dc.bibliographiccitation.volume","6"],["dc.contributor.author","Kuijpers, Petrus F."],["dc.contributor.author","Otte, Matthias"],["dc.contributor.author","Dürr, Maximilian"],["dc.contributor.author","Ivanović-Burmazović, Ivana"],["dc.contributor.author","Reek, Joost N. H."],["dc.contributor.author","de Bruin, Bas"],["dc.date.accessioned","2021-04-29T10:11:23Z"],["dc.date.available","2021-04-29T10:11:23Z"],["dc.date.issued","2016"],["dc.identifier.doi","10.1021/acscatal.6b00283"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/84573"],["dc.relation.issn","2155-5435"],["dc.title","A Self-Assembled Molecular Cage for Substrate-Selective Epoxidation Reactions in Aqueous Media"],["dc.type","journal_article"],["dc.type.internalPublication","no"],["dc.type.subtype","original_ja"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","4880"],["dc.bibliographiccitation.issue","17"],["dc.bibliographiccitation.journal","Chemistry: a European Journal"],["dc.bibliographiccitation.lastpage","4884"],["dc.bibliographiccitation.volume","20"],["dc.contributor.author","Otte, Matthias"],["dc.contributor.author","Kuijpers, Petrus F."],["dc.contributor.author","Troeppner, Oliver"],["dc.contributor.author","Ivanović-Burmazović, Ivana"],["dc.contributor.author","Reek, Joost N. H."],["dc.contributor.author","de Bruin, Bas"],["dc.date.accessioned","2021-04-29T10:11:08Z"],["dc.date.available","2021-04-29T10:11:08Z"],["dc.date.issued","2014-04-22"],["dc.description.abstract","A cobalt-porphyrin catalyst encapsulated in a cubic M8 L6 cage allows cyclopropanation reactions in aqueous media. The caged-catalyst shows enhanced activities in acetone/water as compared to pure acetone. Interestingly, the M8 L6 encapsulated catalyst reveals size-selectivity. Smaller substrates more easily penetrate through the pores of the \"molecular ship-in-a-bottle catalysts\" and are hence converted faster than bigger substrates. In addition, N-tosylhydrazone sodium salts are easy to handle reagents for cyclopropanation reactions under these conditions."],["dc.identifier.doi","10.1002/chem.201400055"],["dc.identifier.pmid","24664657"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/84569"],["dc.language.iso","en"],["dc.relation.eissn","1521-3765"],["dc.relation.issn","0947-6539"],["dc.title","Encapsulated cobalt-porphyrin as a catalyst for size-selective radical-type cyclopropanation reactions"],["dc.type","journal_article"],["dc.type.internalPublication","no"],["dc.type.subtype","original_ja"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","18582"],["dc.bibliographiccitation.issue","34"],["dc.bibliographiccitation.journal","Angewandte Chemie. International Edition"],["dc.bibliographiccitation.lastpage","18586"],["dc.bibliographiccitation.volume","60"],["dc.contributor.author","Bete, Sarah C."],["dc.contributor.author","Otte, Matthias"],["dc.date.accessioned","2021-08-12T07:45:36Z"],["dc.date.available","2021-08-12T07:45:36Z"],["dc.date.issued","2021"],["dc.identifier.doi","10.1002/anie.202106341"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/88505"],["dc.language.iso","en"],["dc.notes.intern","DOI Import GROB-448"],["dc.relation.eissn","1521-3773"],["dc.relation.issn","1433-7851"],["dc.title","Heteroleptic Ligation by an endo ‐Functionalized Cage"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","4172"],["dc.bibliographiccitation.issue","17"],["dc.bibliographiccitation.journal","Organic Letters"],["dc.bibliographiccitation.lastpage","4175"],["dc.bibliographiccitation.volume","17"],["dc.contributor.author","Vliegenthart, Annette B."],["dc.contributor.author","Welling, Frank A. L."],["dc.contributor.author","Roemelt, Michael"],["dc.contributor.author","Klein Gebbink, Robertus J. M."],["dc.contributor.author","Otte, Matthias"],["dc.date.accessioned","2021-04-29T10:11:16Z"],["dc.date.available","2021-04-29T10:11:16Z"],["dc.date.issued","2015-09-04"],["dc.description.abstract","The first shape-persistent macrocycle 1 offering a Brønsted pair functionalized interior is described. Via postcyclization transformation, this heterosequenced compound can be obtained from its corresponding ester 2. The macrocycles differ dramatically in their characteristics such as solubility and appearance. Theoretical investigations suggest that those contrasts might originate from conformational changes due to the formation of a strong O-H-N hydrogen bond in 1."],["dc.identifier.doi","10.1021/acs.orglett.5b01931"],["dc.identifier.pmid","26305263"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/84571"],["dc.language.iso","en"],["dc.relation.eissn","1523-7052"],["dc.relation.issn","1523-7060"],["dc.title","Synthesis and Characterization of a Brønsted Pair Functionalized Shape-Persistent Macrocycle"],["dc.type","journal_article"],["dc.type.internalPublication","no"],["dc.type.subtype","original_ja"],["dspace.entity.type","Publication"]]