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Possible crystallization temperature ranges for a crystallizable miscible polymer blend

Possible crystallization temperature ranges for a crystallizable miscible polymer blend Runt and Martynowicz, 1986 .

Possible curves relating the potential energy in au XH Y hydrogen bonded system with fixed

Possible cycle for a TPAP oxidation step in the synthesis of -batzeUadine A

Possible cyclic action between SRB and SOB

Possible cyclic dianion intermediates 31A-F

Possible cyclic effect of SRB and SOB on a buried pipe

Possible cyclic effect of SRB and SOB on ALWC of steel piles

Possible cyclisation mechanisms in the biosynthesis of trichothecenes and apotrichothecenes the electronic representation is purely indicative, e.g. alcohol nucleophiles may act in their hydroxy rather than alkoxide forms

Possible cyclization modes for geranylgeranyl pyrophosphate.

Possible cyclization reactions of ornithine and lysine.

Possible cycloadducts in the reaction between 2,3-dihydrofuran and benzaldehyde.

Possible cycloadducts in the reaction between 2-furylmethanol and benzaldehyde.

Possible cycloadducts in the reaction between 2-methylfuran and benzaldehyde.

Possible cycloadducts in the reaction between furan and

Possible cycloadducts in the reaction between furan and benzaldehyde.

Possible de-excitation pathways of excited molecules.

Possible decanter configurations.

Possible decay mechanism for J pp.

Possible decision tree to apply in the optimisation of mobile phases for MIPs.

Possible decomposition mechanism involving allyl-silyl exchange.

Possible decomposition mechanism of the polymers TM1 and MP1. Resulting fragments are identified in the mass spectra. REPRINTED WITH PERMISSION OF , COPYRIGHT American Chemical Society

Possible decomposition mechanisms for the acyclic CO2 oligomers

Possible decomposition paths of the cyclic adduct formed by reaction of 2 with azide, N40 release promoted by OH substitution. The cyclic species decomposes to give N20 and N2 in a reaction that is exothermic by 60 kcal mol-1. The structures correspond to single points on the potential hypersurface, calculated at the B3LYP 6-31G level. Relative energies are not drawn to scale. Arrows indicate changes in the molecule that lead to the next step.

Possible decomposition paths of the cyclic adduct formed by reaction of with azide, N4O release promoted by OH substitution. The cyclic species decomposes to give N2O and N2 in a reaction that is exothermic by 60 kcal mol . The structures correspond to single points on the potential hypersurface, calculated at the B3LYP 6-31G level. Relative energies are not drawn to scale. Arrows indicate changes in the molecule that lead to the next step.



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