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Bartlett strength

Bartlett MK, Jones CM, Ryan AE (1942) Vitamin C and wound healing II.. corbie acid content and tensile strength of healing wounds in human beings. N EngJ J Med 226 474-481... [Pg.174]

Figure 8.9 Mean activity coefficients for chlorides and sulfides, plotted following ionic strength of solution. Reprinted from Garrels and Christ (1965), with kind permission from Jones and Bartlett Publishers Inc., copyright 1990. Figure 8.9 Mean activity coefficients for chlorides and sulfides, plotted following ionic strength of solution. Reprinted from Garrels and Christ (1965), with kind permission from Jones and Bartlett Publishers Inc., copyright 1990.
Subsequently Bartlett and colleagues [72,73] made detailed studies of the oxidant strengths of the anions AgF4 and NiF -, of the neutral binary fluorides AgF3 and NiF4, derived from the anions by action of Lewis acids in HF, and of cationic... [Pg.362]

As might be expected, xenon does not form any stroig bonds, bur it does form exothermic compounds with fluorine. Some typical bond strengths are listed in Table 17.1. Bartlett has shown that such values might have been expected by exuapolHUon of known bond energy in related nonmeta] compounds. [Pg.430]

Haque and Kaldor (13), and Pal, Rittby, and Bartlett (14) have reported implementations of methods which incorporate the lowest order effects of triple excitations, here referred to as FSCCSD+T(3) and FSCCSD+T (3), including a few demonstrative results. In this paper, we extend the previous work by presenting detailed equations in the spin orbital framework that allow for the use of both open- (15) and closed-shell reference functions. We then go on to examine the performance of these methods on a much wider range of systems than have been studied previously in order to assess their strengths and weaknesses. [Pg.273]

PE Isotactic polypropylene, PP compatibilized with 5 wt% EPR impact strength Ho Salovey, 1982 Bartlett et a/., 1982... [Pg.540]

Bartlett carried out further work to explore the strength of a hydrogen bond distal from the metal center, between the side-chain carbonyl of Asnll2 and an inhibitor amide NH, by comparing amides and esters such as 3 and 6 (Figure 4). The AAGobs value for these inhibitors is 2.7kcalmol in favor of the amide 3, and in this case... [Pg.3428]


See other pages where Bartlett strength is mentioned: [Pg.346]    [Pg.73]    [Pg.112]    [Pg.74]    [Pg.29]    [Pg.301]    [Pg.597]    [Pg.93]    [Pg.499]    [Pg.1041]    [Pg.508]    [Pg.502]    [Pg.3427]    [Pg.340]   
See also in sourсe #XX -- [ Pg.76 ]




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