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Demand electronics

The first commercial use of tantalum was as filaments ia iacandescent lamps but it was soon displaced by tungsten. Tantalum is used ia chemical iadustry equipment for reaction vessels and heat exchangers ia corrosive environments. It is usually the metal of choice for heating elements and shields ia high temperature vacuum sintering furnaces. In 1994, over 72% of the tantalum produced ia the world went iato the manufacturiag of over 10 x 10 soHd tantalum capacitors for use ia the most demanding electronic appHcations. [Pg.330]

This approach is extremely powerful and endowed with the ability to reach near-atomic resolution. But it is a difficult one to apply in routine analyses because it demands electron microscopic expertise of a high order. It is also a destructive procedure, and not easily adapted for rapid detection and characterization of intergrowths in as-prepared zeolites in general. [Pg.309]

Would a StericaUy demanding, electron-rich ligand like a bulky carbene be the answer ... [Pg.46]

The demanded electron transfer in E. coli RNR could present a real enigma As estimated from the docked complex of the two separately solved three-dimensional structures of R1 and R2 (Figure 4), the site of the stable tyrosyl radical in protein R2 is at a distance of approximately 30n 40 from the active site in protein R1 (Eklund et al 1997 Uhlin and Eklund, 1994). According to theoretical as well as experimental considerations of electron transfer reactions in proteins (Gray and Winkler, 1996 Beratan et al., 1992 Moser et al 1992 Marcus and Sutin, 1985), the electron transfer rate over such a distance would be on the order of InO.OOl s ... [Pg.415]

Electron Demand — Electron Supply) / 2 = Number of Bonds... [Pg.2]

One elegant example of the use of a pseudo-metal ion as a central metal ion, and as a probe, is the study (42) of the electron distribution in the series of tetrahedral complexes of the type R2B(R COCHCOR"). A study of the B resonance indicated the pseudo-metal atom demanded electron donation from the chelate ring in a fixed amount which was found to be a function of R but not of R and R". Because an alteration of the structure of the chelate moiety (either ring size or donor atom) caused changes on the i B and HiNMR of the R2B unit, it was possible to evaluate the electronegativity of the ring system composed of the chelate moiety and the boron atom. [Pg.561]

Chemical oxygen demand ( ) Electron capture detector ( ) Flame ionization detector... [Pg.146]

Alkylation [reaction (3B)] is supported by R being a sterically demanding electron-with-drawing group, R supporting carbenium ion formation. [Pg.457]

Scheme 21). However, when a sterically demanding, electron-withdrawing, trimethylsilyl group is present as a substituent on the ylidic carbon (108c) then no metallation was observed, possibly because ortho-metallation is strongly dependent upon pre-coordination of the lithium ion to the ylide function. [Pg.177]

The stability of the drive oscillation and of the exact demodulation substantially determine the achievable tolerances of the sensor. This requires complex and demanding electronic circuitry. [Pg.302]

Water-soluble derivatives of alkylidenes 8 and 9 were prepared via phosphine ligand substitution reactions. Exchange of the phosphines in 8a for PhP(p-C6H4S03-Na)2 afforded a water-soluble vinyl alkylidene [20]. This alkylidene was soluble in water, but the triarylphosphine ligands were too small and insufficiently electron-donating to produce an active catalyst [48], Analogous substitution of the phosphines in 9 a for more sterically demanding, electron-rich, water-soluble phosphines yielded ruthenium alkylidenes 10 and 11 (Scheme 2), which were soluble in both water and methanol [49]. [Pg.557]

Despite this ubiquitous presence of relativity, the vast majority of quantum chemical calculations involving heavy elements account for these effects only indirectly via effective core potentials (ECP) [8]. Replacing the cores of heavy atoms by a suitable potential, optionally augmented by a core polarization potential [8], allows straight-forward application of standard nonrelativistic quantum chemical methods to heavy element compounds. Restriction of a calculation to electrons of valence and sub-valence shells leads to an efficient procedure which also permits the application of more demanding electron correlation methods. On the other hand, rigorous relativistic methods based on the four-component Dirac equation require a substantial computational effort, limiting their application in conjunction with a reliable treatment of electron correlation to small molecules [9]. [Pg.657]

In the new electronic stmctnres nnder development, interfaces between the various active materials will multiply many-fold. Adhesion in these cases does not merely involve mechanical contact, bnt also demands electronic, ionic, and optical integrity. Thns the stndy of adhesion will become more sophisticated to encompass these new demands. New stmctnred materials will emerge, often with complex self-assembled architectnres. At the nanometer level, it shonld be possible for an electronic device to come together by itself, driven by smart adhesion forces. [Pg.420]

Jayant R Kalagnanam, Andrew J Davenport, and H S Lee. Computational aspects of clearing continous call double auctions with assignment constraints and indivisible demand. Electronic Commerce Journal, 1(3) 221-238, 2001. [Pg.208]

Kalagnanam, J., Devenport, A.J. and H.S. Lee, Computational Aspects of Clearing Continuous Call Double Auctions with Assignment Constraints and Indivisible Demand , Electronic Commerce Journal, 1, 3-15, 2001. [Pg.781]

The Diels-Alder reaction is defined as a [4-1-2] cycloaddition between a conjugated diene and a substituted dienophile (alkene or alkyne) to form a (hetero-)cyclohexene system. Based on the electronic effects of the substituent on the diene and dienophile, Diels-Alder reactions can be classified as normal electron-demand (electron-rich diene reacts with electron-deficient dienophile) or inverse electron-demand (iEDDA, electron-deficient diene reacts with electron-rich dienophile) reactions (Scheme la). In a normal electron-demand Diels-Alder reaction, the electron-deficient dienophile, typically a Michael acceptor, is likely to be attacked by endogenous nucleophiles such as free amino and thiol groups in vivo. For this reason, the use of this reaction in bioorthogonal chemistry apphcations poses a challenge. [Pg.112]

The development of modern technologies demands electronic devices with superior performance reflected in multiplication of their functionality (Tong 2011). One of the challenges in electronic packaging is to overcome barriers concerning thermal management, which is a common problem that can reduce... [Pg.193]

The allylic phosphate (37) and various allylic phosphates bearing steri-cally demanding electron-withdrawing aryl groups have been successfully used in a highly site- and enantioselective Cu-catalyzed allylic alkylation reaction with an easily accessible vinylaluminum reagent to give chiral 8 2 products (Scheme 10). ... [Pg.246]

The use of programmed current waveforms (e.g. periodic current reversal) in order to produce thin, dense, pore<free coatings, particuJarty for demanding electronic applications (section 8.1.2). [Pg.423]

P. A. Janeway, Aluminum Nitride Making the Grade in Demanding Electronic Applications, Ceramic Industry, vol. 137, no. 1, July 1991, pp. 2532. [Pg.62]

Precision components for demanding electronic handling operations such as test sockets that are used to protect delicate devices during robotic handling and high-speed, high-force... [Pg.32]


See other pages where Demand electronics is mentioned: [Pg.10]    [Pg.255]    [Pg.9]    [Pg.17]    [Pg.76]    [Pg.203]    [Pg.27]    [Pg.236]    [Pg.241]    [Pg.57]    [Pg.129]    [Pg.5827]    [Pg.245]    [Pg.640]    [Pg.451]    [Pg.405]    [Pg.554]    [Pg.97]    [Pg.14]    [Pg.160]    [Pg.242]    [Pg.668]    [Pg.35]    [Pg.320]   
See also in sourсe #XX -- [ Pg.8 ]




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1,3-Cycloaddition inverse electron demand

1.2- Diazines, inverse-electron-demand Diels-Alder

1.2- Diazines, inverse-electron-demand Diels-Alder reactions

1.2.4- Triazines inverse-electron-demand

Alkenes inverse electron demand Diels-Alder reactions

Asymmetric Diels-Alder reactions inverse-electron-demand

Catalytic asymmetric inverse-electron-demand

Catalytic asymmetric inverse-electron-demand Diels-Alder reaction

Cycloaddition reaction inverse electron demand

Cycloaddition, Normal-electron demand

Diels electron demand

Diels inverse electron demand

Diels neutral electron demand

Diels normal electron demand

Diels with inverse electron-demand

Diels-Alder reaction electron-demand

Diels-Alder reaction inverse electron demand

Diels-Alder reaction normal electron demand

Diels-Alder reactions reverse electron demand

Diels-Alder reactions with inverse electron demand

Diels-Alder reactions with normal electron demand

Diene inverse electronic demand

Diene synthesis inverse electronic demand

Electron-demand

Electron-demand

Electronic demand

Electronic demand

Electronic demand sensitivity parameter

Electrons lone pairs, steric demands

Halogenation electron-demand

Hetero-Diels-Alder reactions inverse-electron-demand

Increasing electron demand

Increasing electron demand principle

Intramolecular inverse electron demand

Inverse electron demand

Inverse electron demand 1,3-dipolar

Inverse electron demand 1,3-dipolar cycloaddition

Inverse electron demand Diels-Alder carbohydrates

Inverse electron demand Diels-Alder cycloaddition

Inverse electron demand Diels-Alder reactions, examples using

Inverse electron demand aza Diels Alder

Inverse electron demand aza Diels Alder reaction

Inverse electron demand in Diels-Alder reaction

Inverse electron demand using enamines

Inverse electron demand using enols

Inverse electron demand using ketone dithioacetal

Inverse electron-demand Diels-Alder

Inverse electron-demand Diels-Alder Lewis acid catalyzed

Inverse electron-demand Diels-Alder intermolecular

Inverse electron-demand Diels-Alder reactions alkenes, 1,2,4,5-tetrazine

Inverse electron-demand Diels-Alder reactions oxazole

Inverse electron-demand Diels-Alder reactions pyridazine

Inverse electronic demand Diels-Alder

Inverse electronic demand Diels-Alder reaction

Inverse-Electron-Demand Reactions with Enamine-Activated Dienophiles

Inverse-electron-demand hetero

Inverse-electron-demand hetero-Diels-Alder

Inverse-electron-demand hetero-cycloaddition

Inverse-electron-demand ketones

Normal electron demand Diels-Alder

Normal electron-demand

Normal-electron demand reactions

Principle of increasing electron demand

Reactions with Inverse Electron Demand

Retro “inverse electron-demand

Retro “inverse electron-demand Diels-Alder reactions

Reverse electron demand Diels-Alder

Reverse electron-demand type

Reverse electron-demand type Diels-Alder reaction

Reverse electronic demand DielsAlder reaction

Reverse-electron-demand

Subject inverse-electron-demand

Tool of increasing electron demand

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