1595-16-0Relevant articles and documents
MOF-5 as an efficient heterogeneous catalyst for Friedel-Crafts alkylation reactions
Phan, Nam T.S.,Le, Ky K.A.,Phan, Tuan D.
, p. 246 - 253 (2010)
A highly porous metal-organic framework (MOF-5) was synthesized by a solvothermal method, and used as an efficient heterogeneous acid catalyst for Friedel-Crafts alkylation reactions. The solid acid catalyst was characterized using a variety of different techniques, including X-ray powder diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), thermogravimetric analysis (TGA), Fourier transform infrared spectroscopy (FT-IR), atomic absorption spectrophotometry (AAS), and nitrogen physisorption measurements. Quantitative conversion was achieved under mild conditions without the need for an inert atmosphere. The MOF-5 catalyst could be facilely separated from the reaction mixture, and could be reused several times without significant degradation in catalytic activity. Furthermore, no contribution from homogeneous catalysis of active acid species leaching into reaction solution was detected.
METHOD FOR PRODUCING ARENE COMPOUNDS AND ARENE COMPOUNDS PRODUCED BY THE SAME
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Paragraph 0125, (2021/06/26)
Provided is a method for producing (alkyl)arene compounds represented by Formulae 3-1, 3-2, and 3-3 by the Friedel-Crafts alkylation reaction of alkyl halide compounds and arene compounds using organic phosphine compounds as a catalyst.
IRON BISPHENOLATE COMPLEXES AND METHODS OF USE AND SYNTHESIS THEREOF
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Paragraph 00187-00191, (2013/04/25)
The present application, relates to iron bisphenolate complexes and methods of use and synthesis thereof. The iron complexes are prepared from tridentate or tetradentate ligands of Formula I: wherein R1 and R2 are as defined herein. Also provided are methods and processes of using the iron bisphenolate complexes as catalysts in cross-coupling reactions and in controlled radical polymerizations.
Ionic iron(iii) complexes of bis(phenol)-functionalized imidazolium cations: Synthesis, structures and catalysis for aryl Grignard cross-coupling of alkyl halides
Deng, Hai-Ning,Xing, Ya-Lin,Xia, Cong-Liang,Sun, Hong-Mei,Shen, Qi,Zhang, Yong
, p. 11597 - 11607 (2013/02/23)
A series of bis(phenol)-functionalized imidazolium salts, 1,3-bis(4,6-di-R1-2-hydroxybenzyl)-2-R2-4,5-di-R 3-imidazolium chlorides H3LnCl (R1 = tBu, R2 = R3 = H, H3L 1Cl, 1; R1 = CH3, R2 = R3 = H, H3L2Cl, 2; R1 = tBu, R 2 = H, R3 = Cl, H3L3Cl, 3; R 1 = tBu, R2 = CH3, R3 = H, H3L4Cl, 4), were used to produce a novel series of ionic iron(iii) complexes [H3Ln][FeX4] (n = 1, X = Cl, 5; n = 2, X = Cl, 6; n = 3, X = Cl, 7; n = 4, X = Cl, 8; n = 1, X = Br, 9; n = 3, X = Br, 10). All of the complexes were characterized by Raman spectroscopy and electrospray ionization mass spectrometry. Elemental analysis and X-ray crystallography were also used. All of the complexes were non-hygroscopic and air-stable, with five of them existing as solids (5, 7-10) and one as an oil (6) at room temperature. A preliminary catalytic study on the cross-coupling reactions of aryl Grignard reagents with primary and secondary alkyl halides bearing β-hydrogens, revealed that all of the ionic iron(iii) complexes exhibited good to excellent catalytic activity. Complexes 5, 6 and 8 exhibited optimal activity, whereas 7, 9 and 10 showed only moderate activity. Furthermore, by simply decanting the cross-coupling product in the ether layer, complexes 5 and 6 could be reused in at least seven successive runs without significant loss in catalytic activity.