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ABCD block

Scheme 15 Synthesis of poly(aMeSt-fr-pClaMeSt-fr-IB-fr-PVL) linear ABCD block copolymer... Scheme 15 Synthesis of poly(aMeSt-fr-pClaMeSt-fr-IB-fr-PVL) linear ABCD block copolymer...
Abstract This review highlights recent (2000-2004) advances and developments regarding the synthesis of block copolymers with both linear [AB diblocks, ABA and ABC triblocks, ABCD tetrablocks, (AB)n multiblocks etc.] and non-linear structures (star-block, graft, miktoarm star, H-shaped, dendrimer-like and cyclic copolymers). Attention is given only to those synthetic methodologies which lead to well-defined and well-characterized macromolecules. [Pg.15]

Other more complex linear block co-, ter- and quarterpolymers, such as ABC, ABCD, ABABA can be prepared using the previously mentioned methods. An important tool in the synthesis of block copolymers involves the use of post-polymerization chemical modification reactions. These reactions must be performed under mild conditions to avoid chain scission, crosslinking, or degradation, but facile enough to give quantitative conversions. Hydrogenation, hydrolysis, hydrosilylation and quaternization reactions are among the most important post-polymerization reactions used for the preparation of block copolymers. [Pg.19]

The examples where a CFE 2 plan has been divided into two or four blocks are not explicit enough to develop the idea that the relations of the unification of blocks are selected randomly. In the next example, a CFE 2 plan is developed with the purpose being to show the procedures to select the unification relations of inter-blocks. In this plan, the actions showing a systematic influence will be divided into two blocks or into four blocks with, respectively, eight experiments or four experiments per block. We start this new analysis by building the CFE 2 plan. Table 5.64 contains this CFE 2 plan and also gives the division of the two blocks when we use the ABCD interaction as a unification relation. [Pg.444]

If we now suppose that the aim is to divide the CFE plan 2 into four blocks, we can select one of the following unification relations (i) ABCD coupled with one from the three order interactions (ABC, ACD, BCD, etc.) (ii) ABCD coupled with one from the two-order interactions (AB, AC, AD, etc.) (iii) two interactions of three-order, etc. To establish which coupling is the most favourable, it is necessary to know what type of information disappears in each case. For this purpose we show here some of the multiplications of the ABCD interaction relations with their possible coupling interaction relations where A = B = C = D = 1. [Pg.445]

For the synthesis of higher oligosaccharides, two major strategies can be considered. These include the stepwise synthesis and the block synthesis. These two strategies are illustrated for the synthesis of a linear ABCD tetrasaccharide in Scheme 5.2 and Scheme 5.3. [Pg.201]

In the block synthesis, the target oligosaccharide is assembled from a few smaller ohgosaccharides. As shown in Scheme 5.3, for the synthesis of an ABCD oligosaccharide the AB (17) and CD (8) disaccharide blocks are synthesized in parallel and coupled after a single deprotection step (8 9) to afford the protected tetrasaccharide (14). [Pg.203]

Scheme 1-5 Virtual synthetic pathways toward the steroid skeleton with rings A, B, C, and D. Top row stepwise conversion of a ring A (B, C, or D)-building block into the ABCD system middle row expansion in a... Scheme 1-5 Virtual synthetic pathways toward the steroid skeleton with rings A, B, C, and D. Top row stepwise conversion of a ring A (B, C, or D)-building block into the ABCD system middle row expansion in a...
The intermediate AD is a 1,5-diketone and as such accessible by means of a Michael addition of D (as an enolate anion) to A (in a yield of 52%). It is a characteristic of the photochemical synthesis of 123b that the kinetical-ly favored cw-orientation of the ethyl and vinyl groups on the five-membered ring of the Michael adduct AD ensures the thermodynamically disfavored fran -fusion of rings C and D in the Diels-Alder adduct of type ABCD. The overall yield of 123b, based on D, amounts to 11% ). The achiral building block A is accessible by conventional means [118d]. [Pg.271]

The second largest absolute effect value, 9.1 x 10 gcm , occurs for the block effect. The researchers have the options of attributing this value to the water added to the polyol solution, to the ABCD interaction, or to a combination of both. Since four-factor effects are not commonly observed, the suspicion of the researchers seems confirmed the quantity of water in the polyol solution has a distinct effect on the apparent density. This interpretation is consistent with the chemistry of the process, and the observation led to taking precautionary measures for buying, storing and manipulating polyol solutions, to improve the quality of the earplugs produced. [Pg.143]

Four different building blocks incorporated in a single linear macromolecule, named ABCD quaterpolymers, have led to diversity and functionality toward multifunctional nanostruc-tured polymeric materials. [Pg.464]

Consider a 2" factorial experiment with the complete defining relationship I = ABCD. Determine an appropriate blocking pattern for this experiment given that AB is known to be zero, and determine the new complete defining relationship. [Pg.177]

Fig, 7. Collection of building blocks A (achiral) and D (chiral nonracemic), intermediates AD and AD , and main component of Diels/Alder reaction with steroid skeleton ABCD. [Pg.115]

Fig. 27. Evaluation of the steroid synthesis following the constitutional pattern AB-i-D ABCD which gives (+)-estrone after seven steps in an overall yield of 9.6 % (relative to building block AB). Fig. 27. Evaluation of the steroid synthesis following the constitutional pattern AB-i-D ABCD which gives (+)-estrone after seven steps in an overall yield of 9.6 % (relative to building block AB).
Fig. 2.5. A unit cell, ABCD the building block of the lattice. Two sides are of lengths a and b and a is the angle between them... Fig. 2.5. A unit cell, ABCD the building block of the lattice. Two sides are of lengths a and b and a is the angle between them...

See other pages where ABCD block is mentioned: [Pg.144]    [Pg.144]    [Pg.144]    [Pg.144]    [Pg.108]    [Pg.64]    [Pg.260]    [Pg.280]    [Pg.618]    [Pg.298]    [Pg.445]    [Pg.79]    [Pg.13]    [Pg.142]    [Pg.110]    [Pg.140]    [Pg.89]    [Pg.107]    [Pg.609]    [Pg.456]    [Pg.456]    [Pg.457]    [Pg.464]    [Pg.610]    [Pg.132]    [Pg.104]    [Pg.125]    [Pg.127]   
See also in sourсe #XX -- [ Pg.131 ]

See also in sourсe #XX -- [ Pg.131 ]




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