In this work, alkali metal-magnesium aryloxides [MgLi(MesalO)] (1), [MgNa(MesalO)(THF)] for = 2 or 4 (2), and [MgK(MesalO)(THF)] (3) derived from the reaction of MgBu and BuLi, metallic Na or K with methyl salicylate (MesalOH) were used as molecular platforms for the synthesis of new heterometallic compounds [MgLi(EtsalO)] (4), [MgK(EtsalO)] (5), [MgNaAl(MesalO)(OH)(MesalOH)(THF)(HO)] (6), and [MgNa(MesalO)(SalO)(THF)] (7) (EtsalOH = ethyl salicylate and SalOH = salicylic acid) by the reaction with EtOH, exposure to atmospheric moisture or addition of stoichiometric quantities of water. Compounds 4 and 5 were synthesized by transesterification of 1 and 3. Cluster 6 was formed haphazardly by exposing a THF solution of 2 derived using MgBu stabilized with 1 wt% AlEt to atmospheric moisture. Compound 7 was synthesized by partial hydrolysis of 2. Homometallic magnesium aryloxide [Mg(MesalO)(OMe)(HOMe)] (8) was obtained by reaction of MgBu and MesalOH in a methanol solution. The catalytic activity of 1-3 and 6-8 was investigated in the ring-opening polymerization (ROP) of L-lactide (L-LA) or benzaldehyde Tishchenko reaction.
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http://dx.doi.org/10.1039/d2dt00731b | DOI Listing |
Inorg Chem
July 2023
Department of Applied Chemistry, Graduate School of Engineering, Osaka Metropolitan University, 1-1 Gakuen-cho, Naka-ku, Sakai, Osaka 599-8531, Japan.
The new binary sodium magnesium sulfide was prepared by the mechanochemical synthesis route from NaS and MgS as starting materials. NaMgS is extremely sensitive and partially decomposes in the presence of oxygen traces. With the use of an excess of MgS in the milling process, the molar ratio of the impurities was successfully decreased from 38% (NaS + MgO) to 13% MgO.
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June 2022
Faculty of Chemistry, Wrocław University of Science and Technology, 23 Smoluchowskiego, 50-370 Wrocław, Poland.
In this work, alkali metal-magnesium aryloxides [MgLi(MesalO)] (1), [MgNa(MesalO)(THF)] for = 2 or 4 (2), and [MgK(MesalO)(THF)] (3) derived from the reaction of MgBu and BuLi, metallic Na or K with methyl salicylate (MesalOH) were used as molecular platforms for the synthesis of new heterometallic compounds [MgLi(EtsalO)] (4), [MgK(EtsalO)] (5), [MgNaAl(MesalO)(OH)(MesalOH)(THF)(HO)] (6), and [MgNa(MesalO)(SalO)(THF)] (7) (EtsalOH = ethyl salicylate and SalOH = salicylic acid) by the reaction with EtOH, exposure to atmospheric moisture or addition of stoichiometric quantities of water. Compounds 4 and 5 were synthesized by transesterification of 1 and 3. Cluster 6 was formed haphazardly by exposing a THF solution of 2 derived using MgBu stabilized with 1 wt% AlEt to atmospheric moisture.
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March 2015
Key Laboratory of Functional Materials and Devices for Special Environments of CAS; Xinjiang Key Laboratory of Electronic Information Materials and Devices; Xinjiang Technical Institute of Physics & Chemistry of CAS, 40-1 South Beijing Road, Urumqi 830011, China.
A series of alkali metal magnesium tungstates, A4Mg(WO4)3 (A = Na, K), R2Mg2(WO4)3 (R = Rb, Cs), were synthesized from a high temperature solution, and their structures were determined by single-crystal X-ray diffraction. Interestingly, Na4Mg(WO4)3 crystallizes in the monoclinic space group C2/c, while K4Mg(WO4)3 having an identical stoichiometry with Na4Mg(WO4)3, exhibits a different framework structure belonging to triclinic symmetry with the space group P1[combining macron]. Isostructural Rb2Mg2(WO4)3 and Cs2Mg2(WO4)3 crystallize in the space group P213 of cubic symmetry and reveal a three dimensional framework composed of isolated WO4 tetrahedra, MgO6 octahedra and RO12 (R = Rb, Cs) polyhedra.
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March 2008
WestCHEM, Department of Pure and Applied Chemistry, University of Strathclyde, Glasgow, UK.
The reactivity of the Brønsted basic mixed-metal tris-amide compounds of empirical formula [MMg(N(i)Pr2)3] [where M = Li (1), Na (2)] towards phenylacetylene (HC[triple bond, length as m-dash]CPh) has been investigated and has led to the synthesis of a series of mixed-metal acetylido-amido-magnesiates. Thus, 1 and 2 molar equivalents of the alkyne with [MMg(N(i)Pr2)3] produce heteroanionic bis(amido)-mono(acetylido) [LiMg(N(i)Pr2)2(C[triple bond, length as m-dash]CPh)]2 (3) and mono(amido)-bis(acetylido) [(TMEDA) x Na(C[triple bond, length as m-dash]CPh)2Mg(N(i)Pr2)](2) (4) (TMEDA = N,N,N',N'-tetramethylethylenediamine) respectively. X-Ray crystallographic studies reveal that the new compounds adopt a different structural motif.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
August 2007
WestCHEM, Department of Pure and Applied Chemistry, University of Strathclyde, Glasgow, G11XL, UK.
Historically, single-metal organometallic species such as organolithium compounds have been the reagents of choice in synthetic organic chemistry for performing deprotonation reactions. Over the past few years, a complementary new class of metalating agents has started to emerge. Owing to a variable central metal (magnesium, zinc, or aluminum), variable ligands (both in their nature and number), and a variable second metallic center (an alkali metal such as lithium or sodium), "ate" complexes are highly versatile bases that exhibit a synergic chemistry which cannot be replicated by the homometallic magnesium, zinc, or aluminum compounds on their own.
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