Zeitschrift für anorganische und allgemeine Chemie最新文献

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In celebration of the 60th birthday of Rhett Kempe 庆祝瑞特-肯普 60 岁生日
Zeitschrift für anorganische und allgemeine Chemie Pub Date : 2024-06-25 DOI: 10.1002/zaac.202400124
Birgit Weber, Sven Rau
{"title":"In celebration of the 60th birthday of Rhett Kempe","authors":"Birgit Weber, Sven Rau","doi":"10.1002/zaac.202400124","DOIUrl":"https://doi.org/10.1002/zaac.202400124","url":null,"abstract":"","PeriodicalId":23934,"journal":{"name":"Zeitschrift für anorganische und allgemeine Chemie","volume":"193 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-06-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141516319","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Reaction of a Bulky β‐Diketiminato Magnesium Hydride with CO2 Yielding a Polynuclear Magnesium Cage Compound 镁氢化物与二氧化碳反应生成多核镁笼化合物
Zeitschrift für anorganische und allgemeine Chemie Pub Date : 2024-06-24 DOI: 10.1002/zaac.202400070
Wimonsiri Huadsai, Laure Vendier, Matthias Westerhausen, Sébastien Bontemps
{"title":"Reaction of a Bulky β‐Diketiminato Magnesium Hydride with CO2 Yielding a Polynuclear Magnesium Cage Compound","authors":"Wimonsiri Huadsai, Laure Vendier, Matthias Westerhausen, Sébastien Bontemps","doi":"10.1002/zaac.202400070","DOIUrl":"https://doi.org/10.1002/zaac.202400070","url":null,"abstract":"The reaction of a sterically shielded Mg hydride complex, bearing a bulky β‐diketiminato (BDI) ligand, with CO2 leads to the formation of polynuclear complexes. CO2 not only inserts into the metal hydride bond yielding formate ions, but also adds onto the γ‐C of the BDI ligand. This reactivity gives rise to the formation of tri‐ and tetranuclear structures in THF, leading to a hexameric structure associated with a change in the coordination mode of the BDI ligand at 60 °C in THF within four days. The hexameric complex was isolated in high reproducible yield from the solution and characterized by X‐ray diffraction analysis. The reaction affording the hexameric complex was shown to be completed within 1 h at room temperature in toluene. Similar reactions of CO2 with a BDI calcium hydride complex proceeds less cleanly and a pure product could not be isolated.","PeriodicalId":23934,"journal":{"name":"Zeitschrift für anorganische und allgemeine Chemie","volume":"85 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-06-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141506917","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Nominal CaAl2Pt2 and Ca2Al3Pt – two new intermetallic compounds in the ternary system Ca–Al–Pt 名义 CaAl2Pt2 和 Ca2Al3Pt--三元系 Ca-Al-Pt 中的两种新金属间化合物
Zeitschrift für anorganische und allgemeine Chemie Pub Date : 2024-06-24 DOI: 10.1002/zaac.202400094
Stefan Engel, Marcus Koch, Oliver Janka
{"title":"Nominal CaAl2Pt2 and Ca2Al3Pt – two new intermetallic compounds in the ternary system Ca–Al–Pt","authors":"Stefan Engel, Marcus Koch, Oliver Janka","doi":"10.1002/zaac.202400094","DOIUrl":"https://doi.org/10.1002/zaac.202400094","url":null,"abstract":"Single crystals of CaAl2Pt2, Ca2Al3Pt and Ca2AlPt2 were initially observed in an attempt to synthesize Ca3Al4Pt4. Their structures were determined using single‐crystal X‐ray diffraction experiments. While nominal CaAl2Pt2 (CaBe2Ge2 type, P4/nmm, a = 426.79(2), c = 988.79(6) pm, wR2 = 0.0679, 246 F2 values and 18 variables) and Ca2Al3Pt (Mg2Cu3Si type, P63/mmc, a = 561.46(5), c = 876.94(8) pm, wR2 = 0.0664, 214 F2 values and 13 variables) exhibit Al/Pt mixing, for Ca2AlPt2 (Ca2Ir2Si type, C2/c, a = 981.03(2) b = 573.74(1), c = 772.95(2) pm, β = 101.862(1)° wR2 = 0.0307, 2246 F2 values and 25 variables) no mixing was observed. Subsequently, the nominal compositions were targeted with synthetic attempts from the elements using arc‐melting and annealing techniques. For CaAl2Pt2 and Ca2Al3Pt always multi‐phase mixtures were observed while Ca2AlPt2 could be obtained as almost X‐ray pure material. Quantum‐chemical calculations were used to investigate the charge transfer in these compounds rendering them polar intermetallics with a designated [AlxPty]δ– polyanion and Caδ+ cations in the cavities of the polyanions.","PeriodicalId":23934,"journal":{"name":"Zeitschrift für anorganische und allgemeine Chemie","volume":"226 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-06-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141516320","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Synthesis and Reactivity of Amino(ylide)stannylenes 氨基(酰基)锡的合成与反应活性
Zeitschrift für anorganische und allgemeine Chemie Pub Date : 2024-06-20 DOI: 10.1002/zaac.202400079
Varre S. V. S. N. Swamy, Manoj Kumar, Felix Krischer, Kai-Stephan Feichtner, Bert Mallick, Viktoria H. Gessner
{"title":"Synthesis and Reactivity of Amino(ylide)stannylenes","authors":"Varre S. V. S. N. Swamy, Manoj Kumar, Felix Krischer, Kai-Stephan Feichtner, Bert Mallick, Viktoria H. Gessner","doi":"10.1002/zaac.202400079","DOIUrl":"https://doi.org/10.1002/zaac.202400079","url":null,"abstract":"The synthesis of two stable monoylide‐substituted stannylenes of type YCNSnR [R = Cl (1) or N(SiMe3)2 (2), and YCN = Ph3P(CN)C] starting from the cyanido‐substituted α‐metallated ylide YCN‐K and SnCl2 or (SiMe3)2NSnCl is reported. Coordination of the cyano group to the tin center results in the dimerization of both stannylenes 1 and 2 in the solid state as well as in solution, where syn‐ and anti‐isomers are present. X‐ray diffraction analyses in combination with DFT calculations revealed that the π‐electron density of the ylide ligand is predominantly shifted into the cyano moiety rather than towards the tin center. This results in a strong preference of the dimers over the monomers, which is further emphasized by the reaction with 2,5‐di‐tert‐butylhydroquinone, which undergoes a [1+4] addition to the tin center to yield a spiro compound while preserving the cyclic core of the dimer. In contrast, phenyl isocyanate and dicyclohexylcarbodiimide insert into the Sn‐Cylide bond, ultimately leading to the cleavage of the dimer and the formation of monomeric stannylenes with an ylide‐substituted thioamidato and amidinato ligand, respectively.","PeriodicalId":23934,"journal":{"name":"Zeitschrift für anorganische und allgemeine Chemie","volume":"361 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-06-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141530957","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Lewis‐Acid‐Base Synthesis of [Se3Cl3]2[SnCl6] and [BMIm]2[Ga8As6Cl16O14] 路易斯酸碱合成[Se3Cl3]2[SnCl6]和[BMIm]2[Ga8As6Cl16O14]
Zeitschrift für anorganische und allgemeine Chemie Pub Date : 2024-06-20 DOI: 10.1002/zaac.202400092
Claus Feldmann, Maxime A. Bonnin, Michael D. Suedes
{"title":"Lewis‐Acid‐Base Synthesis of [Se3Cl3]2[SnCl6] and [BMIm]2[Ga8As6Cl16O14]","authors":"Claus Feldmann, Maxime A. Bonnin, Michael D. Suedes","doi":"10.1002/zaac.202400092","DOIUrl":"https://doi.org/10.1002/zaac.202400092","url":null,"abstract":"[Se3Cl3]2[SnCl6] (1) and [BMIm]2[Ga8As6Cl16O14] (2) are prepared by Lewis‐acid‐base reaction of SnCl2 with SeCl4 and As2O3 with GaCl3/[BMIm]Cl at room temperature and at 60 °C. 1 contains [ClSe–Se–SeCl2]+ cations with an Se3 unit and isolated octahedral [SnCl6]2– anions. The cation was yet only obtainable via Se0/Se4+ synproportionation in liquid SO2 with AsF5. The [Ga8As6Cl16O14]2– anion in 2 consists of two central edge‐sharing GaO6 octahedra, surrounded by pseudo‐tetrahedral AsO3 units and tetrahedral GaCl3O and GaCl2O2 units. Moreover, an almost planar central Ga4O4 ring surrounded by six GaAs2O3 rings is characteristic, which was not described before. The title compounds are characterized by X‐ray diffraction based on single crystals and powders, infrared spectroscopy, thermogravimetry, and optical spectroscopy.","PeriodicalId":23934,"journal":{"name":"Zeitschrift für anorganische und allgemeine Chemie","volume":"30 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-06-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141516321","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Lithium tris(oxalato)aluminate and its hydrates: structure, mutual transformations and thermal decomposition 三(草酸)铝酸锂及其水合物:结构、相互转化和热分解
Zeitschrift für anorganische und allgemeine Chemie Pub Date : 2024-06-12 DOI: 10.1002/zaac.202400032
Alexander Missyul, Martin Kreuzer, Oleg Usoltsev, Maxim Arsentev, Mikhail Chislov
{"title":"Lithium tris(oxalato)aluminate and its hydrates: structure, mutual transformations and thermal decomposition","authors":"Alexander Missyul, Martin Kreuzer, Oleg Usoltsev, Maxim Arsentev, Mikhail Chislov","doi":"10.1002/zaac.202400032","DOIUrl":"https://doi.org/10.1002/zaac.202400032","url":null,"abstract":"The double oxalates MI3[MIII(C2O4)3] possess rich crystallochemistry and can be used as precursors for various ceramic materials. The article discusses a case of Li3[Al(C2O4)3]. A series of previously unknown hydrates (Li3[Al(C2O4)3]·5.5H2O, Li3[Al(C2O4)3]·4H2O, Li3[Al(C2O4)3]·H2O) was found for this composition, their crystal structure and temperatures of mutual transformations determined. Transformation from Li3[Al(C2O4)3]·4H2O to Li3[Al(C2O4)3]·H2O was found to be accompanied by a change in the topology of the bonding network. Uniaxial negative thermal expansion was found for anhydrous Li3[Al(C2O4)3]. Thermal decomposition of Li3[Al(C2O4)3] was demonstrated to be a promising way to obtain precursors for aluminate ceramics.","PeriodicalId":23934,"journal":{"name":"Zeitschrift für anorganische und allgemeine Chemie","volume":"90 14","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-06-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141352618","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Dynamic Coordination Behavior of a Structurally Constrained, Nucleophilic Sn(II) Towards Gold(I) 受结构限制的亲核 Sn(II) 与金(I)的动态配位行为
Zeitschrift für anorganische und allgemeine Chemie Pub Date : 2024-06-12 DOI: 10.1002/zaac.202400081
Heiko Ruppert, Till Schreyer, M. C. Dietl, Matthias Rudolph, Stephen K. Hashmi, L. Greb
{"title":"Dynamic Coordination Behavior of a Structurally Constrained, Nucleophilic Sn(II) Towards Gold(I)","authors":"Heiko Ruppert, Till Schreyer, M. C. Dietl, Matthias Rudolph, Stephen K. Hashmi, L. Greb","doi":"10.1002/zaac.202400081","DOIUrl":"https://doi.org/10.1002/zaac.202400081","url":null,"abstract":"Tetradentate meso‐octaalkylcalix[4]pyrroles are well‐established ligands in d‐ and f‐block chemistry. In contrast to the related porphyrins, the sp3‐hybridized meso‐carbon atoms linking the four pyrrole units result in highly divers coordination modes. We previously reported on the combination of this ligand system with Sn(II) centers yielding tetracoordinated stannate(II) anions which could be employed as electron‐rich, strong σ‐donor ligands in transition metal chemistry. With this work we are extending the coordination chemistry of meso‐octaethylcalix[4]pyrrolato stannate(II) [1]2− onto gold(I). Synthesis of mono‐ and dinuclear gold complexes reveal a new dynamic binding mode involving μ2‐bridging coordination of a pyrrole nitrogen atom to both Sn and Au. Single‐crystal X‐ray diffraction and variable temperature NMR spectroscopy combined with quantum mechanical computations and bond analysis tools shed light on the involved intermediates.","PeriodicalId":23934,"journal":{"name":"Zeitschrift für anorganische und allgemeine Chemie","volume":"92 11","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-06-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141352595","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Hydrosilylation Reactions with a Dihydrosilylium Ion Stabilized by Coordination of a σ‐Donating Ni(0) Ligand 通过配位σ-供体 Ni(0) 配体稳定的二氢硅烷基离子的氢化反应
Zeitschrift für anorganische und allgemeine Chemie Pub Date : 2024-06-11 DOI: 10.1002/zaac.202400062
Tsuyoshi Kato, Shintaro Takahashi, A. Baceiredo, N. Saffon‐Merceron
{"title":"Hydrosilylation Reactions with a Dihydrosilylium Ion Stabilized by Coordination of a σ‐Donating Ni(0) Ligand","authors":"Tsuyoshi Kato, Shintaro Takahashi, A. Baceiredo, N. Saffon‐Merceron","doi":"10.1002/zaac.202400062","DOIUrl":"https://doi.org/10.1002/zaac.202400062","url":null,"abstract":"The hydrosilylation reactions of dihydrosilylium ion, stabilized by coordination of a σ‐donating Ni(0) fragment, has been investigated. This complex with two reactive sites, dihydrosilylium and Ni(0) centers, readily reacts with diphenylacetylene via a selective mono‐hydrosilylation reaction to afford the corresponding Ni(0)‐stabilized (hydro)(vinyl)silylium ion. In the case of ethylene, three equivalents of olefin are consumed to give a cationic Ni(II)‐complex featuring a Bu‐Si+‐NiII‐Et moiety with a NHC‐supported Si atom. DFT calculations indicate that the hydrosilylation proceeds by a classical (Chalk‐Harrod type) mechanism with the assistance of NHC ligand moving between Si and Ni centers according to their stabilization requirements.","PeriodicalId":23934,"journal":{"name":"Zeitschrift für anorganische und allgemeine Chemie","volume":"72 18","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-06-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141357917","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Synthesis and ligand properties of silsesquioxane‐caged phosphite T7Ph7P 硅倍半氧烷笼型亚磷酸酯 T7Ph7P 的合成和配体特性
Zeitschrift für anorganische und allgemeine Chemie Pub Date : 2024-06-10 DOI: 10.1002/zaac.202400068
Marc Hunsicker, Johannes Krebs, Michael Zimmer, Bernd Morgenstern, Volker Huch, D. Scheschkewitz
{"title":"Synthesis and ligand properties of silsesquioxane‐caged phosphite T7Ph7P","authors":"Marc Hunsicker, Johannes Krebs, Michael Zimmer, Bernd Morgenstern, Volker Huch, D. Scheschkewitz","doi":"10.1002/zaac.202400068","DOIUrl":"https://doi.org/10.1002/zaac.202400068","url":null,"abstract":"The synthesis of the phosphorus‐capped heptaphenylsilsesquioxane T7Ph7P is reported. We show that, unlike previous examples, it readily forms Lewis acid‐base adducts with boranes of different steric demand and the FeCO4 fragment. All complexes were characterized by multinuclear NMR and IR spectroscopy in solution and the solid state. The molecular structures of the adducts with BPh3 and B(C6F5)3 were determined from XRD suitable single crystals. The relative conformation of the Ph and C6F5 rings in T7Ph7P‐B(C6F5)3 suggests favorable π‐interactions, stabilizing the adducts to such a degree that attempts to activate H2 or CO2 were unsuccessful.","PeriodicalId":23934,"journal":{"name":"Zeitschrift für anorganische und allgemeine Chemie","volume":"112 38","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-06-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141362365","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
The Mixed‐Anion compound La2S2(CN2) 混合阴离子化合物 La2S2(CN2)
Zeitschrift für anorganische und allgemeine Chemie Pub Date : 2024-06-10 DOI: 10.1002/zaac.202400038
Hans Jürgen Meyer, Markus Stöbele, Albert T Schwarz
{"title":"The Mixed‐Anion compound La2S2(CN2)","authors":"Hans Jürgen Meyer, Markus Stöbele, Albert T Schwarz","doi":"10.1002/zaac.202400038","DOIUrl":"https://doi.org/10.1002/zaac.202400038","url":null,"abstract":"The new binary metal carbodiimide La2S2(CN2) was synthesized via solid‐state metathesis reaction. The crystal structure was solved and refined on basis of single‐crystal X‐ray diffraction data with space group C2/m. The structure is represented by a layered structure, based on alternating layers of lanthanum, sulfide, and carbodiimide units. A close resemblance of the structure with that of La2O2C2 is discussed, as well as the less‐common coordination number seven of the lanthanum atom.","PeriodicalId":23934,"journal":{"name":"Zeitschrift für anorganische und allgemeine Chemie","volume":"121 20","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-06-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141360528","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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