Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Oxides bonding

Aluminum, the most common material used for contacts, is easy to use, has low resistivity, and reduces surface Si02 to form interfacial metal-oxide bonds that promote adhesion to the substrate. However, as designs reach submicrometer dimensions, aluminum, Al, has been found to be a poor choice for metallization of contacts and via holes. Al has relatively poor step coverage, which is nonuniform layer thickness when deposited over right-angled geometric features. This leads to keyhole void formation when spaces between features are smaller than 0.7 p.m. New collimated sputtering techniques can extend the lower limit of Al use to 0.5-p.m appHcations. [Pg.348]

EtO)2P(S)] with short oxide bonds and phosphate oxygen weakly bridging to the second tin. This relates to the carboxylate structure of (26b) where the additional bridges are weaker. [Pg.132]

Disulfide bonds arise when the SH groups of two cysteine residues are covalently linked as a dithiol by oxidation. Bonds of this type are only found (with a few exceptions) in extracellular proteins, because in the interior of the cell glutathione (see p.284) and other reducing compounds are present in such high concentrations that disulfides would be reduc-... [Pg.72]

Figure 1 Crystal structure of 2,5-dihydro-2,4- Figure 2 Crystal structure of 2,4-diphenyi-2/7-diphenyl-l,2,3,5-thiatriazole 1-oxide (bond lengths in 1,2,3,5-thiatriazol-l-ium bromide (bond lengths in A A and bond angles in °). and bond angles in °). Figure 1 Crystal structure of 2,5-dihydro-2,4- Figure 2 Crystal structure of 2,4-diphenyi-2/7-diphenyl-l,2,3,5-thiatriazole 1-oxide (bond lengths in 1,2,3,5-thiatriazol-l-ium bromide (bond lengths in A A and bond angles in °). and bond angles in °).
In oxides a large departure from the stoichiometric composition is usually met. The importance of this phenomenon, also for the understanding of the oxide bond, is highlighted at the end of the chapter. [Pg.75]

Here, the main features of the valence band results for Th02 and UO2 will be illustrated. Since a large number of publications exists in this field (especially for uranium oxides), reference will be made only to a few selected investigations, chosen for the purpose of highlighting those aspects of the oxide bond discussed previously. A very comprehensive review of these results can be found (and references therein electronic and spectroscopic properties in Refs. 109-111). Figure 21 shows the photoemission spectrum of Th02 and UO2 up to Et = 45 eV The valence band region extends to about 10 eV. The marked difference is the appearance in UO2 of a sharp and intense peak at Et =... [Pg.240]

Which Metal Oxide Bonds Are Critical for Oxidation Reactions V=0, V-O-V or V-O-Support ... [Pg.39]

Toluene p-sulfonyl hydrazones (tosyl hydrazones) undergo C=N oxidative bond cleavage with H202 in the presence of TS-1, to give high yields of the corresponding carbonyl compounds very likely, the reaction proceeds through... [Pg.316]


See other pages where Oxides bonding is mentioned: [Pg.172]    [Pg.953]    [Pg.352]    [Pg.222]    [Pg.95]    [Pg.88]    [Pg.431]    [Pg.431]    [Pg.386]    [Pg.132]    [Pg.78]    [Pg.15]    [Pg.15]    [Pg.296]    [Pg.236]    [Pg.117]    [Pg.296]    [Pg.521]    [Pg.247]    [Pg.203]    [Pg.397]    [Pg.41]    [Pg.1081]    [Pg.293]    [Pg.240]    [Pg.443]    [Pg.50]    [Pg.316]    [Pg.104]    [Pg.20]    [Pg.273]    [Pg.138]   
See also in sourсe #XX -- [ Pg.117 , Pg.126 , Pg.148 ]




SEARCH



1.2.5- Oxadiazole-2-oxides, calculated bond

1.2.5- Oxadiazole-2-oxides, calculated bond tautomerisation

Alane bonds oxidative addition

Allylic C-H bonds oxidation

Aluminium oxide monolayer bonding

Aluminum oxide bond energy

Aluminum oxide reaction bonding

Amine oxides bonding

Azomethine bond oxidation

Bond Graph Modelling of a Solid Oxide Fuel Cell

Bond angles ethylene oxide

Bond cleavage, oxidative addition

Bond distances ethylene oxide

Bond formation oxidative

Bond lengths oxides

Bond metal/oxide

Bond oxidative

Bond oxidative addition reactions

Bond oxidatively induced

Bonded films lead oxide

Bonding ethylene oxide

Bonding metal oxide catalysts

Bonding oxidation reactions

Bonding oxidation states

Bonding oxidative addition

Bonding states, copper oxides

Bonds oxidative addition

Bonds polonium oxides

Bonds selenium oxides

Borane bonds oxidative addition

Borane bonds oxidative cleavage

Boron oxide bonding

Butane. Oxidation at secondary and primary C—H bonds

Butanoic acid via oxidation of carbon-tin bonds

C-CN Bond Cleavage via Oxidative Addition

C-H bond oxidative addition

CH bond oxidations

Carbon, bonding oxidation states

Carbon-boron bonds oxidation

Carbon-boron bonds oxidative cleavage

Carbon-hydrogen bonds cleavage, anodic oxidation

Carbon-hydrogen bonds oxidative addition

Carbon-hydrogen bonds, oxidation

Carbon-mercury bonds oxidation

Carbon-metal bonds oxidation

Carbon-metal bonds oxidative formation

Carbon-metal bonds, oxidations, copper©) acetate

Carbon-nitrogen bond forming reactions oxidative cyclization

Carbon-nitrogen bonds oxidation additions

Carbon-nitrogen bonds oxidation enantioselectivity

Carbon-nitrogen bonds oxidation synthesis

Carbon-oxygen bonds oxidation additions

Carbon-oxygen bonds oxidation enantioselectivity

Carbon-oxygen bonds oxidation synthesis

Carbon-palladium bonds oxidation

Carbon-selenium bonds oxidation

Carbon-silicon bonds oxidative cleavage

Cerium oxides structure-bonding

Chemical Bonding in Cyclic-cluster Model Local Properties of Composite Crystalline Oxides

Covalent bonding oxidation states

Covalent bonds molecules with, oxidation states

Covalent bonds, oxidative addition

C—H bonds, oxidation

Directed metal oxidation reaction-bonding process

Disulfide bonds oxidation

Disulfide bonds oxidizing lipids

Double bond migration Oppenauer oxidation

Double bond, oxidation allylic

Double bonds oxidation

Double bonds oxidative cleavage

Early History of C-H Bond Oxidative Addition

Eliminations to Form Carbon-Oxygen Double Bonds Oxidation Reactions

Ester-bond cleavage, oxidative

Four-Stage Oxide-Bond-Forming Kinetics

Graphite Modification by Mild Oxidation and Chemically Bonded (CB) SEI

Hydride bonds, oxidative addition

Hydrogen bonding, nitrile oxide cycloadditions

Hydrogen peroxide, bond order oxidation

Hydrogen-Bonded Pyridine N-Oxides

Hydrogenation, of a double bond over copper chromium oxide

Inhibitor-oxide bond

James Bond, Oxidative Stress, and Antioxidant Phenols

Magnesium oxide, bond energy

Manganese oxidation carbon-hydrogen bonds

Mercuric oxide bonds

Metal oxidation processing reaction bonding

Metal oxides poly bonding

Metal—carbon bonding oxidative-addition reactions

Metal—carbon triple bonds oxidation reactions

Microbial Oxidation of Non-activated C-H Bond

Microbial oxidation unactivated C—H bonds

Multiple bonds oxidation

Nature of metal-oxide bond

Nezukone via oxidation of carbon-tin bonds

Nitric oxide, insertion into metal-carbon bonds

Nitrile oxides double bonds

Nitrogen oxide bond lengths

Nitrogen oxide three-electron bond

Oxidation C-H bond activation

Oxidation activated C—H bonds

Oxidation and nitration of C-N bonds

Oxidation at the Double Bond of Allylic Alcohols

Oxidation bonds

Oxidation by C-H Bond Cleavage

Oxidation carbon-halogen bonds

Oxidation carbon-silicon bonds

Oxidation of Alkynes Involving No Bond Cleavage

Oxidation of Benzylic C-H Bonds

Oxidation of C-H Bonds in Alkanes

Oxidation of C-H bonds

Oxidation of Saturated Unactivated and Activated C-H Bonds

Oxidation of Unsaturated Alcohols at Multiple Bonds

Oxidation of Unsaturated Ethers at Multiple Bonds

Oxidation of carbon-hydrogen bond

Oxidation of the C-H bond in acetals

Oxidation triple bond formulation

Oxidation unactivated C—H bonds

Oxidation unsaturated bond oxidations

Oxidation, of double bonds

Oxidations of C-N bonds

Oxidative Addition and C — H Bond Activation

Oxidative Addition of Alkane CH Bonds to Organometallics

Oxidative Addition to B—H Bonds

Oxidative Additions Involving Ligand Bond Cleavage

Oxidative Bond-cleavage Processes

Oxidative addition of C-H bond

Oxidative addition of N-H bond

Oxidative addition of alkane C-H bonds

Oxidative addition of the carbon-halogen bond

Oxidative addition of the formyl C-H bond

Oxidative addition of the ortho C-H bond

Oxidative cleavage bonds

Oxidative cleavage, of double bonds

Oxidative generation bond cleavage

Oxidative generation bond dissociation

Oxidative rearrangements bonds

Oxidative rearrangements carbon-hydrogen bond activation

Oxides and bonding

Oxides carbon—hydrogen bonds

Oxides chemical bonding

Oxides silicon-phosphorus bonds

Oxides, bond energies

PDMS, bonding oxidation

Phosphorus—silicon bonds carbon oxides

Quadruple bonds oxidation

Reaction-bonded aluminum oxide (RBAO

Reaction-bonding process oxidation

Reductive and Oxidative Bond-cleavage Reactions

Reductive and Oxidative Bond-formation Reactions

Silicon-hydrogen bond oxidation

Solid binary oxides, structure-bonding

Solid mixed oxides, structure-bonding

Sulfides oxidative carbon-sulfur bond cleavage

Sulfur, bond oxidation states

Sulfur, bond strengths oxidation states

Trimethylamine N-oxide C—Si bonds

Trimethylamine oxide, bonding

Valency and oxidation numbers a historical sketch of bonding theory prior to quantum mechanics

Wacker oxidation C—O bond formation

Zinc oxide poly bonding

Zinc oxide rubber-metal bonding

© 2024 chempedia.info