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Ring living

Play with those frequencies for awhile, though, and you ll find you can push the overtones into complex chords. Such chords have a ringing, live sound and contain more than three notes. Interesting effects can also be created by tuning one or more voices slightly off-key. [Pg.225]

The RRDE is very usefiil for the detection of short-lived intemiediates, in the investigation of reaction iiiechanisms, but also in the distinction of free and adsorbed intemiediates, as tiie latter are not transported to the ring. [Pg.1937]

Barbituric acid is the parent of a group of compounds known as barbiturates The bar biturates are classified as sedative-hypnotic agents meaning that they decrease the responsiveness of the central nervous system and promote sleep Thousands of deriva lives of the parent ring system of barbituric acid have been tested for sedative-hypnotic activity the most useful are the 5 5 disubstituted derivatives... [Pg.900]

Ring-Opening Metathesis Polymerization. Several new titanacyclobutanes have been shown to initiate living ring-opening metathesis polymerization (ROMP) systems. These have been used to make diblock and triblock copolymers of norbomene [498-66-8] (N) and its derivatives (eg, dicyclopentadiene [77-73-6] (D)) (Fig. 2) (41). [Pg.181]

Most reactions leading to isoxazoles must involve at some stage cyclization of an intermediate which contains all five atoms of the isoxazole ring. In some cases the acyclic intermediates are short-lived and unisolable, in others they are stable and able to be isolated. In this section we discuss reactions which involve an isolable acyclic precursor. These reactions mostly utilize (CCCNO) synthons although a few examples of (OCCCN), (CCCON) and (CONCC) synthons are encountered. We are unaware of examples involving (CNOCC) synthons. [Pg.73]

The occurrence of nucleophilic participation is also indicated by a rate enhancement relative to the rate of solvolysis of n-butyl p-bromobenzenesulfonate. The solvolysis rates of a series of cu-mefhoxyall l p-bromobenzenesulfontes have been determined. A maximum rate is again observed where participation of a methoxy group via a live-membered ring is possible (see Table 5.20). [Pg.311]

The stabilizing influence in the hydrated cation is the amidinium resonance. If a solution of the cation is neutralized, a short-lived hydrated neutral molecule (4) (half-life 9 sec at pH 10) is obtained with an ultraviolet spectrum similar to that of the hydrated cation but shifted to longer wavelengths (5 m/ ). Supporting evidence can be derived from the anhydrous nature of the cation of 4-nitroiso-quinoline (pK 1.35), in which the nitro group has a similar electronic influence to that of the ring nitrogen atom N-I in quinazoline and where amidinium resonance is not possible. [Pg.257]

Inclusion of oxygen on the pyrimidine ring has been found empirically to increase the effective serum half-lives. [Pg.129]

The solubility of calcium carbonate is such that in a saturated solution the product of ion concentrations [Ca+2][C0 2] is 5 X I0 B. Though this may seem quite small, it is large enough to be important to man, especially if he lives in a region of the earth where there are extensive limestone deposits. Calcium carbonate can be dissolved in water, especially if it contains much dissolved C02. This is objectionable because soap added to water which contains even traces of Ca+2 forms a precipitate of calcium stearate. This is the ring that is so difficult to remove from the bathtub. [Pg.384]

Living Radical Polymerization Table 9.1 Five-Membered Ring Nitroxides for NMP... [Pg.473]

How can you use the rotating ring disk electrode for detecting short-lived intermediate species ... [Pg.139]

When the ring system containing the sulfone moiety is unsaturated, a quite different set of products has been observed on photolysis, apparently arising from an initial cycloreversion to a short-lived sulfene intermediate. For example, irradiation of 2H-1-benzothiopyran 1,1-dioxide (41) in dichloromethane or methanol gave the cis- and trans-sultines (42) and the ring-expanded sultine (43) in roughly equal amounts, accompanied by minor amounts ( 5%) of the products of formal loss of S02, i.e. indene, and SO, i.e. 4472... [Pg.882]


See other pages where Ring living is mentioned: [Pg.5]    [Pg.657]    [Pg.1937]    [Pg.292]    [Pg.168]    [Pg.355]    [Pg.1]    [Pg.352]    [Pg.116]    [Pg.189]    [Pg.53]    [Pg.174]    [Pg.1208]    [Pg.400]    [Pg.510]    [Pg.134]    [Pg.13]    [Pg.164]    [Pg.89]    [Pg.331]    [Pg.806]    [Pg.49]    [Pg.1197]    [Pg.92]    [Pg.72]    [Pg.91]    [Pg.680]    [Pg.602]    [Pg.113]    [Pg.451]    [Pg.715]    [Pg.751]    [Pg.2]    [Pg.2]    [Pg.11]    [Pg.24]    [Pg.38]    [Pg.28]    [Pg.50]   
See also in sourсe #XX -- [ Pg.141 ]

See also in sourсe #XX -- [ Pg.561 ]




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Addition-ring-opening living

Addition-ring-opening living polymerization

Living cationic ring-only

Living cationic ring-only polymerization

Living polymers ring opening metathesis polymerization

Living ring opening metathesis

Living ring opening metathesis polymerization

Nucleophilic living ring-opening

Nucleophilic living ring-opening polymerization

Ring opening polymerization living anionic

Ring-opening polymerization living character

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