Triphenylbismuth diacylates as novel reagents for fine organic synthesis

Triphenylbismuth diacylates, Ph₃Bi(O₂CR)₂ (R = Me, Et, Ph, CF₃, CH=CH₂), are novel effective reagents for fine organic synthesis. They oxidize primary and secondary alcohols and di-tert-glycols under mild conditions to form the corresponding carbonyl compounds in high yields;O- andN-phenylate alcohols, enols, and amines; andO- ando-C-phenylate phenols.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 12, pp. 2043–2047, December, 1993.     

Palladium-catalyzed reaction of some triphenylbismuth(V) sulfonates and phenolates with methyl acrylate

Triphenylbismuth(V) derivatives Ph₃BiX₂ [X = OC₆H₂(NO₂)₃-2,4,6, OC₆H₂(NO₂-4)Br₂-2,6, OTs, OSO₂C₆H₄OH-4] react with methyl acrylate and PdCl₂ (1:3:0.04 molar ratio) in acetonitrile at 20°C to form the cross-coupling products, methyl cinnamate (0.26–0.51 mol mol^?1 starting bismuth compound) and methyl hydrocinnamate (0–0.17 mol mol^?1); diphenyl, the homocoupling product (0–0.13 mol mol^?1); and benzene (0.02–0.15 mol mol^?1). The reaction of Ph₃Bi(OSO₂C₆H₄OH-4)₂ is characterized by the selective formation of methyl cinnamate, but the reagent activity is low. Ph₃Bi(OTs)₂ exhibits the highest activity among the derivatives studied, but the reaction selectivity is low. The mechanisms of the palladium-catalyzed formation of homo-and cross-coupling products are proposed.     

Syntheses of antimony(v) derivatives from trimethyl and triphenylantimony(III), dihydric phenols,andtert-butyl hydroperoxide

Trimethyl and triphenylantimonyo-phenylene dioxides were obtained by the reaction of trimethyl- and triphenylantimony with pyrocatechol in the presence oftert-butyl hydroperoxide in 68 and 81 % yields, respectively. 7,7,7,15,15,15-Hexamethyl-(and phenyl)-6,8,14,16-tetraoxa-7, 15-distibatricyclo[11.3.1.1^9,13]octadeca-1,3,5,9,11,13-hexaenes were synthesized analogously by the reaction with resorcinol (in 79 and 93 % yields, respectively). The use of hydroquinone resulted in polymeric trimethyl- and triphenylantimony hydroquinolates.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 4, pp. 748–751, April, 1995.This work was carried out with financial support from the Russian Foundation for Basic Research (Project No 94-03-08846).     

Cluster oxalate complexes [M3(mu3-Q)(mu2-Q2)3(C2O4)3]2- and [Mo3(mu3-Q)(mu2-Q)3(C2O4)3(H2O)3]2- (M = Mo, W; Q = S, Se): mechanochemical synthesis and crystal structure

Mechanochemical reaction of cluster coordination polymers 1infinity[M3Q7Br4] (M = Mo, W; Q = S, Se) with solid K2C2O4 leads to cluster core excision with the formation of anionic complexes [M3Q7(C2O4)3]2-. Extraction of the reaction mixture with water followed by crystallization gives crystalline K2[M3Q7(C2O4)3].0.5KBr.nH2O (M = Mo, Q = S, n = 3 (1); M = Mo, Q = Se, n = 4 (2); M = W, Q = S, n = 5 (3)). Cs2[Mo3S7(C2O4)3].0.5CsCl.3.5H2O (4) and (Et4N)1.5H0.5K{[Mo3S7(C2O4)3]Br}.2H2O (5) were also prepared. Close Q...Br contacts result in the formation of ionic triples {[M3Q7(C2O4)3](2)Br}5- in 1-4 and the 1:1 adduct {[Mo3S7(C2O4)3]Br}3- in 5. Treatment of 1 or 2 with PPh(3) leads to chalcogen abstraction with the formation of [Mo3(mu3-Q)(mu2-Q)3(C2O4)3(H2O)3]2-, isolated as (Ph4P)2[Mo3(mu3-S)(mu2-S)3(C2O4)3(H2O)3].11H2O (6) and (Ph4P2[Mo3(mu3-Se)(mu2-Se)3(C2O4)3(H2O)3].8.5H2O.0.5C2H5OH (7). All compounds were characterized by X-ray structure analysis. IR, Raman, electronic, and 77Se NMR spectra are also reported. Thermal decomposition of 1-3 was studied by thermogravimetry.     

Synthesis and structure of Ta4S9Br8. An emergent family of early transition metal chalcogenide clusters

Single crystals of Ta4S9Br8 are obtained by heating Ta, S, and Br2 at 400 degrees C in a 4.0:9.0:4.0 molar ratio in a 44% yield. The structure was determined by X-ray analysis and consists of molecular clusters [Ta4(mu4-S)(mu-S2)4Br8]. The tantalum atoms form a square with long Ta...Ta distances (3.30 angstroms), with four S2 ligands bridging the Ta-Ta edges and one capping the square. Each Ta atom has two terminal bromine atoms. The compound is diamagnetic and has only two electrons for metal-metal bonding. IR and Raman spectral studies with the use of 34S allow to identify characteristic vibrations S-S (537 cm(-1)) and Ta4-mu4-S (407 cm(-1)). The compound is soluble in CH3CN, giving a dark-red solution with a characteristic electronic spectrum, which was assigned on the base of DFT calculations. ESI-MS spectra of the solutions show formation of [[Ta4S9Br8]Br]- associates.     

Synthesis and reactivity of W3Te74+ clusters and chalcogen exchange in the M3Q7 (M = Mo, W; Q = S, Se, Te) cluster family

Heating WTe(2), Te, and Br(2) at 390 degrees C followed by extraction with KCN gives [W(3)Te(7)(CN)(6)](2-). Crystal structures of double salts Cs(3.5)K{[W(3)Te(7)(CN)(6)]Br}Br(1.5).4.5H(2)O (1), Cs(2)K(4){[W(3)Te(7)(CN)(6)](2)Cl}Cl.5H(2)O (2), and (Ph(4)P)(3){[W(3)Te(7)(CN)(6)]Br}.H(2)O (3) reveal short Te(2)...X (X = Cl, Br) contacts. Reaction of polymeric Mo(3)Se(7)Br(4) with KNCSe melt gives [Mo(3)Se(7)(CN)(6)](2-). Reactions of polymeric Mo(3)S(7)Br(4) and Mo(3)Te(7)I(4) with KNCSe melt (200-220 degrees C) all give as final product [Mo(3)Se(7)(CN)(6)](2)(-) via intermediate formation of [Mo(3)S(4)Se(3)(CN)(6)](2-)/[Mo(3)SSe(6)(CN)(6)](2-) and of [Mo(3)Te(4)Se(3)(CN)(6)](2-), respectively, as was shown by ESI-MS. (NH(4))(1.5)K(3){[Mo(3)Se(7)(CN)(6)]I}I(1.5).4.5H(2)O (4) was isolated and structurally characterized. Reactions of W(3)Q(7)Br(4) (Q = S, Se) with KNCSe lead to [W(3)Q(4)(CN)(9)](5-). Heating W(3)Te(7)Br(4) in KCNSe melt gives a complicated mixture of W(3)Q(7) and W(3)Q(4) derivatives, as was shown by ESI-MS, from which E(3)[W(3)(mu(3)-Te)(mu-TeSe)(3)(CN)(6)]Br.6H(2)O (5) and K(5)[W(3)(mu(3)-Te)(mu-Se)(3)(CN)(9)] (6) were isolated. X-ray analysis of 5 reveals the presence of a new TeSe(2-) ligand. The complexes were characterized by IR, Raman, electronic, and (77)Se and (125)Te NMR spectra and by ESI mass spectrometry.     

Oxidation of Pt-bound bis-hydroxylamine as a novel route to unexplored dinitrosoalkane ligated species

The reaction of K 2[PtCl 4] and HO(H)NCMe 2CMe 2N(H)OH.H 2SO 4 ( BHA.H 2SO 4; 2) in a molar ratio 1:2 at 20-25 degrees C in water affords a mixture of [Pt(BHA) 2][PtCl 4] ( 5) and [Pt(BHA-H) 2] ( 6) ( BHA- H = anionic monodeprotonated form of BHA) which, upon heating at 80-85 degrees C for 12 h or on prolonged keeping at 20-25 degrees C for 2 weeks, is subject to a slow transformation giving [PtCl 2(BHA)] ( 7). The latter compound is also obtained from the reaction between K[PtCl 3(Me 2 SO)] and 2. The chlorination of [PtCl 2(BHA)] ( 7) in freshly distilled dry chloroform leads to the selective oxidation of one N(H)OH group yielding [PtCl 2{HO(H) NCMe 2CMe 2 N=O}] ( 13), while the chlorination in water produces the complex [PtCl 2(O= NCMe 2CMe 2 N=O)] ( 14) bearing the unexplored dinitrosoalkane species. Treatment of 14 with 2 equiv of 1,2-bis-(diphenylphosphino)ethane (dppe) in CH 2Cl 2 results in the liberation of the dinitrosoalkane ligand followed by its fast cyclization giving the alpha-dinitrone (3,3,4,4-tetramethyl-1,2-diazete-1,2-dioxide) in solution and the solid [Pt(dppe) 2](Cl) 2. The Pt (II) complexes with hydroxylamino ( intersection)oximes [PtCl 2{HO(H) NC(Me) 2C(R)= NOH}] (R = Me 8; R = Ph 9) upon their oxidation with Cl 2 in CHCl 3 afford the nitrosoalkane derivatives [PtCl 2{O= NCMe 2C(R)= NOH}] (R = Me 16; Ph 17), respectively, while the corresponding chlorination of the bis-chelates [Pt{HO(H) NCMe 2C(R)= NOH} 2] (R = Me 10; Ph 11) gives [Pt{O= NCMe 2C(R)= NO} 2] (R = Me 18; Ph 19). The formulation of 5- 19 is based on C, H, and N microanalyses, IR, 1D ( (1)H, (13)C{ (1)H}, (195)Pt) and 2D ( (1)H, (1)H-COSY, (1)H, (13)C-HSQC) NMR spectroscopies, and X-ray diffraction for five complexes ( 5, 7, and 12- 14).     

Destruction of 2,4-Dichlorophenol in Water Solution Using a Combined Process of Sorption and Plasma Exposure to DBD

The results of studies of the decomposition of 2,4-dichlorophenol (2,4-DCP) in its aqueous solution under the action of atmospheric pressure DBD in an oxygen flow are presented. A new reactor design was used in which the discharge zone was filled with a sorbent (diatomite). It was found that the kinetics of decomposition obeys a first-order kinetic equation for the concentration of 2,4-DCP. The presence of an adsorbent significantly improves the parameters of the decomposition process. Decomposition rates, rate constants and energy efficiency are doubled. So, at a specific discharge power of 1.8 W/cm³ in the presence of a sorbent, the rate constant was ~1 s^?1, and without it, ~0.5 s^?1. The energy efficiency was 0.031 and 0.016 molecules per 100 eV, respectively. The parameters of the treated solution are improved in terms of its potential toxicity. The concentrations of the main decomposition products (aldehydes, carboxylic acids) in the presence of a sorbent are significantly less than without it. This is due to an increase in the rate of conversion of these products into carbon dioxide molecules. It was also shown that the decomposition of one 2,4-DCP molecule leads to the formation of two chloride ions in solution, and the ozone formed in the discharge does not significantly affect the destruction process.

     

Magnetorefractive effect in granular films with tunneling magnetoresistance

The magnetorefractive effect, consisting in a change of reflectivity under magnetization, has been observed in granular Co-Al-O metal-insulator magnetic films with tunneling magnetoresistance in the IR region. It is shown that this effect manifests itself most clearly in interference conditions, is even in magnetization, and reaches as high as 0.8% at frequencies of about 1100 cm^?, which exceeds both the linear equatorial Kerr and the even orientational magneto-optic effects by an order of magnitude.