Maurice Conrad, Sebastian Bette, Robert E. Dinnebier, Thomas Schleid
{"title":"On the Thermal Dimorphy of the Strontium Perrhenate Sr[ReO4]2","authors":"Maurice Conrad, Sebastian Bette, Robert E. Dinnebier, Thomas Schleid","doi":"10.1002/zaac.202400045","DOIUrl":"https://doi.org/10.1002/zaac.202400045","url":null,"abstract":"Hygroscopic single crystals of a new hexagonal high‐temperature modification of Sr[ReO<jats:sub>4</jats:sub>]<jats:sub>2</jats:sub> were prepared from a melt of Sr[ReO<jats:sub>4</jats:sub>]<jats:sub>2</jats:sub> ⋅ H<jats:sub>2</jats:sub>O and SrCl<jats:sub>2</jats:sub> ⋅ 6 H<jats:sub>2</jats:sub>O. The structure analysis of the obtained crystals by X‐ray diffraction revealed that the title compound crystallizes in the ThCd[MoO<jats:sub>4</jats:sub>]<jats:sub>3</jats:sub>‐type structure with the hexagonal space group <jats:italic>P</jats:italic>6<jats:sub>3</jats:sub>/<jats:italic>m</jats:italic> and the lattice parameters <jats:italic>a</jats:italic>=1023.81(7) pm and <jats:italic>c</jats:italic>=646.92(4) pm (<jats:italic>c</jats:italic>/<jats:italic>a</jats:italic>=0.632) for <jats:italic>Z</jats:italic>=2 in its quenchable high‐temperature form. Two crystallographically independent Sr<jats:sup>2+</jats:sup> cations are coordinated by oxygen atoms forming either octahedra or tricapped trigonal prisms, whereas the Re<jats:sup>7+</jats:sup> cations are found in the centers of discrete tetrahedral <jats:italic>meta</jats:italic>‐perrhenate units [ReO<jats:sub>4</jats:sub>]<jats:sup>−</jats:sup>. Temperature‐dependent <jats:italic>in‐situ</jats:italic> PXRD studies of dry powder samples of Sr[ReO<jats:sub>4</jats:sub>]<jats:sub>2</jats:sub> exhibited its thermal dimorphy with a phase‐transition temperature at 500–550 °C from literature‐known m‐Sr[ReO<jats:sub>4</jats:sub>]<jats:sub>2</jats:sub> into the newly discovered h‐Sr[ReO<jats:sub>4</jats:sub>]<jats:sub>2</jats:sub> (hexagonal).","PeriodicalId":23934,"journal":{"name":"Zeitschrift für anorganische und allgemeine Chemie","volume":"35 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-06-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141506915","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}
Harbi Tomah AL-Masri, Suzan Mohammed Alrawashdeh, Akram Ali Almejled, Ziad moussa
{"title":"Synthesis and crystal structures of novel group 6B metal carbonyl complexes with N‐(4‐methyl‐2‐ pyridinyl)‐P,P‐diphenylphosphinous amide ligand","authors":"Harbi Tomah AL-Masri, Suzan Mohammed Alrawashdeh, Akram Ali Almejled, Ziad moussa","doi":"10.1002/zaac.202400075","DOIUrl":"https://doi.org/10.1002/zaac.202400075","url":null,"abstract":"The reaction of N‐(4‐methyl‐2‐pyridinyl)‐P,P‐diphenylphosphinous amide ligand 4‐Me‐C5H3N‐2‐NH(PPh2) (1) with M(CO)6 (M = Cr, Mo, W) in refluxing toluene afforded a mononuclear group 6B metal tetracarbonyls [M(CO)4{1‐κ2P,N}] (M = Cr(2), Mo(3), W(4) ). Complexes 2–4 were characterized by multinuclear NMR (1H, 13C and 31P NMR) and IR spectroscopy, and their structures were also determined by single crystal X‐ray diffraction. 2 and 4 represent the first examples of structurally characterized complexes of such ligands with group 6B metal carbonyls.","PeriodicalId":23934,"journal":{"name":"Zeitschrift für anorganische und allgemeine Chemie","volume":"23 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-06-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141506916","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}
{"title":"The peculiar molecular [(IF5)6(HF2)4]4− anion of the compound K4[(IF5)6(HF2)4]","authors":"Björn Koch, Tim Florian Graubner, Florian Kraus","doi":"10.1002/zaac.202400085","DOIUrl":"https://doi.org/10.1002/zaac.202400085","url":null,"abstract":"K4[(IF5)6(HF2)4] was obtained from the reaction of K[HF2] with liquid IF5. The compound was analyzed by single crystal and powder X‐ray diffraction, Raman spectroscopy, and quantum‐chemical calculations. It contains the largest molecular IF5/HF2− complex anion known so far. Surprisingly, the crystal structure of the A4B compound can be related to the Hg4Pt structure type.","PeriodicalId":23934,"journal":{"name":"Zeitschrift für anorganische und allgemeine Chemie","volume":"180 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-06-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141506918","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}
Jingyao Yang, Feiyu Lu, Wencui Li, Lu Zhang, Jingrui Yin, Mohd. Muddassir, Liming Fan
{"title":"Practicality and Compatibility of Cd(II) Coordination Polymer as Luminescent Sensor in Selective and Sensitive Detection of 3‐Nitrotyrosine Biomarker","authors":"Jingyao Yang, Feiyu Lu, Wencui Li, Lu Zhang, Jingrui Yin, Mohd. Muddassir, Liming Fan","doi":"10.1002/zaac.202400065","DOIUrl":"https://doi.org/10.1002/zaac.202400065","url":null,"abstract":"Based on the mixed ligands of 1,4‐bis(2,4,6‐tricarboxylpyrid‐5‐yl)benzene (H6BTPB) and 1,4‐bis(imidazol‐1‐yl)benzene (bib), a new cadmium(II) coordination polymer with the molecular formula of {[Cd(bib)(μ2‐H2O)(H2O)2](H4BTPB)0.5(bib)0.5}n (CdCP) was constructed under solvothermal condition, and displayed a 3D supramolecular structure expanded by the hydrogen bonds between the 1D [Cd(bib)(μ2‐H2O)(H2O)2]n ladder chain and the guests. Profiting from its superior stability and inherent luminescence, the prepared CdCP dispalyed great potential as a highly sensitive and selective luminescent sensor in trace detection of 3‐NT biomarker in both water and real bodily fluids through the luminescence quenching effects, with the Ksv and LODs being 2.408×105 M‐1 and 30.3 nM in water, 2.230×105 M‐1 and 44.7 nM in diluted urine, 2.249×105 M‐1 and 43.9 nM in diluted serum, respectively. Subsequent mechanism studies indicated the synergistic effect of internal filtering effect, photo‐induced electron transfer, and fluorescence resonance energy transfer determining the luminescence quenching response of CdCP towards 3‐NT biomarker.","PeriodicalId":23934,"journal":{"name":"Zeitschrift für anorganische und allgemeine Chemie","volume":"15 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-06-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141516318","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}
{"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}
{"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}
{"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}
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}
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}
Aihaimaitijiang Ababaikeri, Gulimeikereyi Tuniyazi, Yanhui Zhang, D. S. Malik
{"title":"Ba<sub>3</sub>Zn<sub>4</sub>Si<sub>4</sub>O<sub>15</sub>: A Novel Centrosymmetric Silicate with Isolated SiO<sub>4</sub> and Si<sub>2</sub>O<sub>7</sub> Units","authors":"Aihaimaitijiang Ababaikeri, Gulimeikereyi Tuniyazi, Yanhui Zhang, D. S. Malik","doi":"10.1002/zaac.202400026","DOIUrl":"https://doi.org/10.1002/zaac.202400026","url":null,"abstract":"Abstract A new silicate Ba 3 Zn 4 Si 4 O 15 (BZSO), was synthesized by the high‐temperature solution method in the open air, and the structure was determined using single‐crystal X‐ray diffraction data. The compound can be regarded as a derivative of α‐SiO 2 tetrahedral framework. The structural analysis indicates that it crystallizes in the centrosymmetric space group C 2/ c (No. 15) with lattice parameters a =19.3931(12) Å, b =5.1262(4) Å, c =16.3620(12) Å, β =115.7°, V =1465.5 Å 3 , Z =4 of a monoclinic crystal system composed of isolated Si 2 O 7 dimers, and SiO 4 , ZnO 4 tetrahedra. Experimental characterization demonstrates that it possesses birefringence of 0.013@546.1 nm. Besides, the first‐principles theoretical calculations were carried out to elucidate the relationship between the electronic structure and optical property.","PeriodicalId":23934,"journal":{"name":"Zeitschrift für anorganische und allgemeine Chemie","volume":"650 18","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-06-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/zaac.202400026","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147895295","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}