Cleavage of ether-oxygen bond in phenoxyacetic acid by an Arthrobacter species

1968 ◽  
Vol 16 (3) ◽  
pp. 538-539 ◽  
Author(s):  
Charles S. Helling ◽  
Jean Marc. Bollag ◽  
J. E. Dawson
Keyword(s):  
Phenoxyacetic Acid ◽  
Ether Oxygen ◽  
Arthrobacter Species ◽  
Oxygen Bond

Conformations of Bridged Diphenyls. I. Crystal Structure of 2-(3′-Methyl-4′-nitrophenoxy)-1,3-diisopropylbenzene

1972 ◽  
Vol 50 (18) ◽  
pp. 2963-2971 ◽  
Author(s):  
E. A. H. Griffith ◽  
W. D. Chandler ◽  
B. E. Robertson
Keyword(s):  
Bond Angle ◽  
The Other ◽  
X Ray Diffraction ◽  
Hexagonal Symmetry ◽  
X Ray ◽  
Ether Oxygen Atom ◽  
Phenyl Rings ◽  
Ether Oxygen ◽  
Independent Molecules ◽  
Oxygen Bond

The structure of 2-(3′-methyl-4′-nitrophenoxy)-1,3-diisopropylbenzene, C19H23NO3, has been determined by X-ray diffraction. The crystals are triclinic, a = 12.422(24), b = 13.180(25), c = 11.241(30) Å, α = 89.99(20), β = 95.81(15), γ = 105.46(12)°, [Formula: see text] with Z = 4. The intensities of 8153 independent reflections were measured on a four circle diffractometer, of which 3701 were used in the refinement of the structure to give a final least-squares weighted residue of 0.053.The ether oxygen bond angle in each of the two independent molecules is 120°. The two phenyl rings are nearly orthogonal in each case, while the ring containing the electron withdrawing nitro group is conjugated with the ether oxygen atom. The rings show significant deviations from hexagonal symmetry and the nitro-substituted ring is bent away from the other ring.

Oxygen-Oxygen Bond Cleavage and Formation in Co(II) Mediated Stoichiometric O2 Reduction via the Potential Intermediacy of a Co(IV) Oxyl Radical

2018 ◽  
Author(s):  
Lucie Nurdin ◽  
Denis M. Spasyuk ◽  
Laura Fairburn ◽  
Warren Piers ◽  
Laurent Maron
Keyword(s):  
Bond Cleavage ◽  
Peroxo Complex ◽  
Oxygen Oxygen ◽  
O2 Reduction ◽  
Oxygen Bond ◽  
Pentadentate Ligand

Diprotonation of a remarkably stable, toluene soluble cobalt peroxo complex supported by a neutral, dianionic pentadentate ligand leads to facile O-O bond cleavage and production of a highly reactive Co(IV) oxyl cation intermediate that dimerizes and releases O<sub>2</sub>. These processes are relevant to both O<sub>2</sub> reduction and O<sub>2</sub> evolution and the mechanism was probed in detail both experimentally and computationally.

Formation of Carbon-Oxygen Bond Mediated by Hypervalent Iodine Reagents Under Metal-free Conditions

2020 ◽  
Vol 17 ◽  
Author(s):  
Ayesha Jalil ◽  
Yaxin O Yang ◽  
Zhendong Chen ◽  
Rongxuan Jia ◽  
Tianhao Bi ◽  
...  
Keyword(s):  
Natural Products ◽  
Bond Formation ◽  
Building Blocks ◽  
Review Article ◽  
Hypervalent Iodine ◽  
Metal Free ◽  
Bioactive Natural Products ◽  
The Past ◽  
Oxygen Bond ◽  
Privileged Scaffolds

: Hypervalent iodine reagents are a class of non-metallic oxidants have been widely used in the construction of several sorts of bond formations. This surging interest in hypervalent iodine reagents is essentially due to their very useful oxidizing properties, combined with their benign environmental character and commercial availability from the past few decades ago. Furthermore, these hypervalent iodine reagents have been used in the construction of many significant building blocks and privileged scaffolds of bioactive natural products. The purpose of writing this review article is to explore all the transformations in which carbon-oxygen bond formation occurred by using hypervalent iodine reagents under metal-free conditions

Participation of 19-ester groups in the cleavage of 2α,3α- and 5α,6α-steroid epoxides. A case of competition between participation and external nucleophile attack

1979 ◽  
Vol 44 (5) ◽  
pp. 1496-1509 ◽  
Author(s):  
Pavel Kočovský ◽  
Václav Černý
Keyword(s):  
Perchloric Acid ◽  
Hydrobromic Acid ◽  
Ester Group ◽  
Carbonyl Oxygen ◽  
Cyclic Carbonate ◽  
Cyclic Ether ◽  
Normal Reaction ◽  
Neighboring Group ◽  
Ether Oxygen ◽  
The Difference

Acid cleavage of the acetoxy epoxide IIIa with aqueous perchloric acid or hydrobromic acid gave two types of products, i.e. the diol Va or the bromohydrin VIa, and the cyclic ether VIII. The latter compound arises by participation of ether oxygen of the ester group. On reaction with perchloric acid the epoxide IVa gave the diol XIIIa as a product of a normal reaction and the isomeric diol Xa as a product arising by intramolecular participation of the carbonyl oxygen of the 19-acetoxy group. Participation of the 19-ester group is confirmed by the formation of the cyclic carbonate XI when the 19-carbonate IVb is treated analogously. On reaction with hydrobromic acid, the epoxide IVa gave solely the bromohydrin XIVa as a product of the normal reaction course. Discussed is the similarity of these reactions with electrophilic additions to the related 19-acetoxy olefins I and II, the mechanism, the difference in behavior of both epoxides III and IV, the dependence of the product ratio on the nucleophility of the attacking species, and the competition between participation of an ambident neighboring group and an external nucleophile attack.

Crystal structure of tamsulosin hydrochloride, C20H29N2O5SCl

2021 ◽  
pp. 1-7
Author(s):  
Nilan V. Patel ◽  
Joseph T. Golab ◽  
James A. Kaduk ◽  
Amy M. Gindhart ◽  
Thomas N. Blanton
Keyword(s):  
Crystal Structure ◽  
Hydrogen Bond ◽  
Hydrogen Atom ◽  
Powder Diffraction ◽  
Density Functional ◽  
Carbon Chain ◽  
Strong Hydrogen Bond ◽  
Powder Diffraction File ◽  
Ether Oxygen ◽  
Sulfonamide Group

The crystal structure of tamsulosin hydrochloride has been solved and refined using synchrotron X-ray powder diffraction data and optimized using density functional techniques. Tamsulosin hydrochloride crystallizes in space group P21 (#4) with a = 7.62988(2), b = 9.27652(2), c = 31.84996(12) Å, β = 93.2221(2)°, V = 2250.734(7) Å3, and Z = 4. In the crystal structure, two arene rings are connected by a carbon chain oriented roughly parallel to the c-axis. The crystal structure is characterized by two slabs of tamsulosin hydrochloride molecules perpendicular to the c-axis. As expected, each of the hydrogens on the protonated nitrogen atoms makes a strong hydrogen bond to one of the chloride anions. The result is to link the cations and anions into columns along the b-axis. One hydrogen atom of each sulfonamide group also makes a hydrogen bond to a chloride anion. The other hydrogen atom of each sulfonamide group forms bifurcated hydrogen bonds to two ether oxygen atoms. The powder pattern is included in the Powder Diffraction File™ as entry 00-065-1415.

scholarly journals Structure, thermal stability and magnetic behavior of Mn(II) complexes with phenoxyacetic acid herbicides

Polyhedron ◽  
2021 ◽  
pp. 115370
Author(s):  
Aleksandra Drzewiecka–Antonik ◽  
Wiesława Ferenc ◽  
Barbara Mirosław ◽  
Dariusz Osypiuk ◽  
Jan Sarzyński
Keyword(s):  
Thermal Stability ◽  
Magnetic Behavior ◽  
Phenoxyacetic Acid ◽  
Acid Herbicides

scholarly journals Nanostructural Arrangements and Surface Morphology on Ureasil-Polyether Films Loaded with Dexamethasone Acetate

Nanomaterials ◽  
2021 ◽  
Vol 11 (6) ◽  
pp. 1362
Author(s):  
Joao Augusto Oshiro ◽  
Angelo Lusuardi ◽  
Elena M. Beamud ◽  
Leila Aparecida Chiavacci ◽  
M. Teresa Cuberes
Keyword(s):  
Film Surface ◽  
Crystalline Phases ◽  
Essential Information ◽  
X Ray ◽  
Force Microscopy ◽  
Ether Oxygen ◽  
Dexamethasone Acetate ◽  
Poly Ethylene ◽  
The One ◽  
Poly Propylene

Ureasil-Poly(ethylene oxide) (ureasil-PEO500) and ureasil-Poly(propylene oxide) (u-PPO400) films, unloaded and loaded with dexamethasone acetate (DMA), have been investigated by carrying out atomic force microscopy (AFM), ultrasonic force microscopy (UFM), contact-angle, and drug release experiments. In addition, X-ray diffraction, small angle X-ray scattering, and infrared spectroscopy have provided essential information to understand the films’ structural organization. Our results reveal that while in u-PEO500 DMA occupies sites near the ether oxygen and remains absent from the film surface, in u-PPO400 new crystalline phases are formed when DMA is loaded, which show up as ~30–100 nm in diameter rounded clusters aligned along a well-defined direction, presumably related to the one defined by the characteristic polymer ropes distinguished on the surface of the unloaded u-POP film; occasionally, larger needle-shaped DMA crystals are also observed. UFM reveals that in the unloaded u-PPO matrix the polymer ropes are made up of strands, which in turn consist of aligned ~180 nm in diameter stiffer rounded clusters possibly formed by siloxane-node aggregates; the new crystalline phases may grow in-between the strands when the drug is loaded. The results illustrate the potential of AFM-based procedures, in combination with additional physico-chemical techniques, to picture the nanostructural arrangements in polymer matrices intended for drug delivery.

Edge‐confined Pt1/MoS2 single‐atom catalyst promoting the selective activation of carbon‐oxygen bond

ChemCatChem ◽  
2021 ◽  
Author(s):  
Yang Lou ◽  
Yi Zhao ◽  
Hong Liu ◽  
Qingqing Gu ◽  
Bing Yang ◽  
...  
Keyword(s):  
Single Atom ◽  
Selective Activation ◽  
Oxygen Bond
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