saint+ v8.38a integration engine, data reduction software (Bruker Corporation)
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saint+ v8.38a integration engine, data reduction software
Saint+ V8.38a Integration Engine, Data Reduction Software, supplied by Bruker Corporation, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/data+reduction+software+saint/saint++v8+38a+integration+engine/pmc10107310__ANIE___62___0___s001-316-9-12
Average 90 stars, based on 1 article reviews
Saint+ V8.38a Integration Engine, Data Reduction Software, supplied by Bruker Corporation, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/data+reduction+software+saint/saint++v8+38a+integration+engine/pmc10107310__ANIE___62___0___s001-316-9-12
Average 90 stars, based on 1 article reviews
saint+ v8.38a integration engine, data reduction software - by Bioz Stars,
2026-09
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other:Article Title: Crystal X-ray Diffraction and Molecular Modeling Considerations Elucidate the Factors Responsible for the Opposing Host Behavior of Two Isostructural Xanthenyl- and Thioxanthenyl-Derived Host Compounds Article Snippet: In this work, we compare the host behaviour of two structurally related compounds, N,N'-bis(9phenyl-9-xanthenyl)ethylenediamine and N,N'-bis(9-phenyl-9-thioxanthenyl)ethylenediamine when each one was recrystallized from mixtures of guest solvents pyridine, morpholine, piperidine and dioxane. (These solvents were clathrated individually in single solvent experiments.). In these conditions, the two hosts displayed distinctly opposing selectivities: when employing an equimolar quaternary guest mixture, the resulting mixed complex of the oxygen host analogue contained a significant amount of dioxane (68%) and only 8% pyridine, while the sulfur host derivative discriminated inordinately against dioxane (12%) in favour of pyridine (57%).. These results were more remarkable when considering the crystal packing of the two apohost compounds, which revealed them to be isostructural. Software:Article Title: Oxidation of dimethylplatinum(II) complexes with a peroxyacid. Article Snippet: The complexes [PtMe2(NN)], NN = 2,2’-bipyridine = bipy, 1a; NN = di-2-pyridylamine = dpa, 1b; NN = di-2pyridyl ketone = dpk, 1c, NN = 4,4’-bis(ethoxycarbonyl)-2,2’-bipyridine, bebipy, react with m-chloroperoxybenzoic acid to give the platinum(IV) complexes [Pt(OH)(O2C-3-C6H4Cl)Me2(NN)], NN = bipy, 2, or [Pt(OH)(OH2⋯O2C-3-C6H4Cl)Me2(NN)], NN = bipy, 3a; dpa, 3b; bebipy, 3d, or [Pt(OH)2Me2(dpkOH)]3[Pt(OH)-(OH2)Me2(dpkOH)][H(O2C-3-C6H4Cl)2]·2MeOH, 43·5·2MeOH.. The reactions are proposed to occur by a polar oxidative addition mechanism, followed in most cases by the coordination of water.. Complex 3a crystallises as a supramolecular polymer, the compound 43·5·2MeOH crystallises as a supramolecular sheet structure, and 3d easily forms a gel, all through strong intermolecular hydrogen bonding. Article Title: Carbon–Hydrogen versus Nitrogen–Oxygen Bond Activation in Reactions of N-Oxide Derivatives of 2,2′-Bipyridine and 1,10-Phenanthroline with a Dimethylplatinum(II) Complex Article Snippet: The reactions of the potential oxygen atom donor ligands 1,10-phenanthroline N-oxide (phenO) and 2,2′-bipyridine N-oxide (bipyO) with the dimethylplatinum(II) complex [Pt2Me4(μ-SMe2)2] are reported.. The reaction with the more rigid ligand phenO gave [PtMe2(κ N,O-phenO)], which underwent oxidative addition with 4-tBu-C6H4CH2Br to give the platinum(IV) complex [PtBrMe2(CH2C6H4-4t-Bu)(phenO)].. The complex [PtMe2(phenO)] reacted with methanol in air to give [Pt(OH)(OMe)Me2(phenO)], but under an inert atmosphere it gave [Pt(OH)(OMe)Me2(phen)], in a reaction involving N−O bond activation. Article Title: Hydrothermal Synthesis and Structure of Coordination Polymers by Combination of Bipyrazole and Aromatic Dicarboxylate Ligands Article Snippet: Nine new coordination polymers, namely 2 ¥[Ag(Hp2CA)(Me4bpz)] (I), 3 ¥[Zn2(p2CA)2(Me4bpz)] (II), 2 ¥[Cd(OAc)2(Me4bpz)(H2O)] (III), 1 ¥[Ag2(m2CA)(Me4bpz)2] (IV), 3 ¥[Zn(m2CA)(Me4bpz)] (V), 2 ¥[Cd(m2CA)(Me4bpz)] 3H2O (VI), 1 ¥[Ag(OAc)(Me4bpz)2] 3 5.4 H2O (VII), 3 ¥[Zn2(OHm2CA)2(Me4bpz)2] 3 1.75 H2O (VIII), and 2 ¥[Cd(OHm2CA)(Me4bpz)(H2O)] (IX) [Hp2CA, terephthalic acid monoanion; p2CA, terephthalic acid dianion; OAc, acetate; m2CA, isophthalic acid dianion; OHm2CA, 5-hydroxy-isophthalic acid dianion; Me4bpz, 3,3 0,5,50-tetramethyl-4,40-bipyrazole], were obtained from acetate hydrates of Agþ, Zn2þ, and Cd2þ and mixed ligand systems consisting ofMe4bpz and the respective aromatic dicarboxylic acid by means of hydrothermal synthesis.. The compounds were characterized by means of X-ray single-crystal structure analysis, elemental analysis, and IR spectroscopy.. The topologies realized in these coordination polymers vary from simple onedimensional polymers to complex three-dimensional frameworks. Article Title: A host–guest approach to combining enzymatic and artificial catalysis for catalyzing biomimetic monooxygenation Article Snippet: SMART, Data collection software (version 5.629) (Bruker AXS Inc., Madison, WI, 2003). .. SAINT, |