Sodium condensed electron

The condensed electron configuration for a nitrogen atom, for example, is [He]2s 2p. The notation [He] is used to represent Is. For a sodium atom [Z = 11), the condensed electron configuration is [Ne]3s. Here, [Ne] represents, ls 2s 2p . Be aware that condensed electron configurations are simply convenient short forms. Thus, [Ne]3s does not mean that a sodium atom is the same as a neon atom plus one electron. Sodium and neon are different elements because the nuclei of their atoms are completely different. 

The sodium condensation reaction of a,co-bis(chlorosilyl)-substituted compounds and the coupling reaction of dilithio derivatives of compounds bearing 7t-electron systems with dichlorosilanes offer a convenient route to various silicon containing polymers. However, the polymers prepared by these methods always contain a small proportion of siloxy units in the polymer backbone, which would interrapt the electron delocalisation. Therefore, new synthetic routes to organosilicon polymers have been developed in which no alkali metal halide condensations are involved [6, 7]. We report syntheses of organosilicon... 

When alkali metal atoms are co-condensed with strong electron acceptors in matrices, electron transfer occurs spontaneously, as discussed above in the case of K + O3. If not spontaneous, electron transfer can easily be activated by photolysis. Irradiation by the Nao line (583 nm cf. ionization energy corresponding to 243 kJmol ) is sufficient to transfer the sodium valence electron to several molecular substrates e.g., CI2 CI2, B2H6 B2Hft, HI -> H + I. ... 

In Group IA(1), lithium and sodium have the condensed electron configuration [noble gas] ns (where n is the quantum number of the outermost energy level), as do all the other alkali metals (K, Rb, Cs, Fr). All are highly reactive metals that form ionic compounds with nonmetals with formulas such as MCI, M2O, and M2S (where M represents the alkali metal), and all react vigorously with water to displace H2. 

We can generalize what we have just done for the electron configuration of sodium. In writing the condensed electron configuration of an element, the electron configuration of the nearest noble-gas element of lower atomic number is represented by its chemical symbol in brackets. For lithium, for example, we write... 

We refer to the electrons represented by the bracketed symbol as the noble-gas core of the atom. More usually, these inner-shell electrons are referred to as the core electrons. The electrons given after the noble-gas core are called the outer-shell elearons. The outer-shell electrons include the electrons involved in chemical bonding, which are called the valence electrons. For the elements with atomic number of 30 or less, all of the outer-shell electrons are valence electrons. By comparing the condensed electron configurations of lithium and sodium, we can appreciate why these two elements are so... 

The sodium condensation reaction of compounds involving two chlorosilyl groups attached to a thiophene ring offers a convenient route to silicon-containing polymers in which a regular alternating arrangement of disilanylene unit and n electron system is found in the polymer backbone. This synthetic route was first used by Weber [58] and was also studied by Ishikawa [60]. It is summarized in Scheme 14.17. 

Butyroin has been prepared by reductive condensation of ethyl butyrate with sodium in xylene, or with sodium in the presence of chloro-trimethylsilane. and by reduction of 4,5-octanedlone with sodium l-benzyl-3-carbamoyl-l,4-dihydropyridine-4-sulfinate in the presence of magnesium chloride or with thiophenol in the presence of iron polyphthalocyanine as electron transfer agent.This acyloin has also been obtained by oxidation of (E)-4-octene with potassium permanganate and by reaction of... 

Condensation between aldehyde 40 and amine 29 followed by sodium borohydride reduction of the resultant imine and cyclisation yielded isoquinoline 41 in good yield. Cyclisation occurred exclusively at the more electron-rich aromatic group. 

Phenyl indandiones With an acidic hydrogen often interfere with clot formation. When electron withdrawing groups are present in the p-position, acidity is increased and activity goes up. The opposite effect is seen with electron-donating substituents. Synthesized in the usual way, the anticoagulant bromindione (15) results from sodium acetate-catalyzed condensation of phthalic anhydride and p-a-bromophenyl-acetic acid. ... 

Similar nucleophilic addition of electrons can also occur to the carbonyl carbon atom of diesters such as (62), e.g. from sodium in solvents such as xylene, but the resultant dianion (63) differs from (59) in possessing excellent leaving groups, e.g. eOEt, and the overall result is the acyloin condensation ... 

In the general context of donor/acceptor formulation, the carbonyl derivatives (especially ketones) are utilized as electron acceptors in a wide variety of reactions such as additions with Grignard reagents, alkyl metals, enolates (aldol condensation), hydroxide (Cannizzaro reaction), alkoxides (Meerwein-Pondorff-Verley reduction), thiolates, phenolates, etc. reduction to alcohols with lithium aluminum hydride, sodium borohydride, trialkyltin hydrides, etc. and cyloadditions with electron-rich olefins (Paterno-Buchi reaction), acetylenes, and dienes.46... 

Examples of the Michael-type addition of carbanions, derived from activated methylene compounds, with electron-deficient alkenes under phase-transfer catalytic conditions have been reported [e.g. 1-17] (Table 6.16). Although the basic conditions are normally provided by sodium hydroxide or potassium carbonate, fluoride and cyanide salts have also been used [e.g. 1, 12-14]. Soliddiquid two-phase systems, with or without added organic solvent [e.g. 15-18] and polymer-supported catalysts [11] have been employed, as well as normal liquiddiquid conditions. The micellar ammonium catalysts have also been used, e.g. for the condensation of p-dicarbonyl compounds with but-3-en-2-one [19], and they are reported to be superior to tetra-n-butylammonium bromide at low base concentrations. 

One-electron reduction of unsaturated a,8-diketones may sometimes generate a diene structure and initiate condensation. Thus, triazoledions (TAD) pass into tetraazabicyclooctanetetraones (TABO). Naphthalene-sodium (ca. 1 mol%), sodium metal, or even sodium iodide efficiently catalyzes the reaction. Tetracyanoethyene and lead tetraacetate retard it. Consequently, the condensation has a chain character (Borhani and Greene 1986 Scheme 7.30). 

The sp-valent metals such as sodium, magnesium and aluminium constitute the simplest form of condensed matter. They are archetypal of the textbook metallic bond in which the outer shell of electrons form a gas of free particles that are only very weakly perturbed by the underlying ionic lattice. The classical free-electron gas model of Drude accounted very well for the electrical and thermal conductivities of metals, linking their ratio in the very simple form of the Wiedemann-Franz law. However, we shall now see that a proper quantum mechanical treatment is required in order to explain not only the binding properties of a free-electron gas at zero temperature but also the observed linear temperature dependence of its heat capacity. According to classical mechanics the heat capacity should be temperature-independent, taking the constant value of kB per free particle. 

The electronic interaction is small if the metal used as an adsorbent has a work function low in relation to the polarizability of the adsorbed atoms. On adsorption of sodium atoms on an aluminum surface of = 4.08 volts, for instance, Brady and Jacobsmeyer (56) obtained a noticeable increase of the photoelectric emission only after five atom layers of sodium had been condensed. In this case the alkali layer itself and not the metal of the sublayer emitted the electrons. 

Perhaps the most useful part of the reported synthesis is the facile preparation of (—)-pyrimidoblamic acid (12 Scheme 3). A key to this synthesis is the preparation of the fully substituted pyrimidine 8. This was done by a one-pot inverse electron demand Diels-Alder reaction between the symmetrical triazine 7 and prop-1-ene-1,1-diamine hydrochloride, followed by loss of ammonia, tautomerization, and loss of ethyl cyanoformate through a retro-Diels-Alder reaction. Selective low-temperature reduction of the more electrophilic C2 ester using sodium borohydride afforded 9, the aldehyde derivative of which was condensed with 7V -Boc-protected (3-aminoalaninamide to give the imine 10. Addition of the optically active A-acyloxazolidinone as its stannous Z-enolate provided almost exclusively the desired anti-addition product 11, which was converted into (—)-pyrimidoblamic acid (12). Importantly, this synthesis confirmed Umezawa s assignment of absolute configuration at the benzylic center. 

A study carried out with various K-region arene oxides shows that the reactivity order of epoxides with sodium cresolate in DMSO is 29 > 28 > 1, 253 > 4 > 254. The poor regioselectivity observed in the reactions of 28 and 29 with the cresolate is attributed to the insensitivity of the reaction to electronic influences as well as by the inherent absence of the electronic effects on the condensed benzo ring.24... 

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