Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Bibliography and Notes for Section 4.2 Chiral Dendrimers

According to the majority rules model the chirality of the enantiomer of the chiral monomer present in excess is amplified during polymerisation [38] (Fig. 4.78). Even if just a small enantiomeric excess is present, the resulting polymer shows a helical inequality identical to that of the corresponding chiral homopolymer (see the caption of Fig. 4.78 for details). [Pg.165]

Both effects (sergeant/soldier and majority rules) require helical conformations of the polymer strands undergoing formation (with mobile helical points of inversion). [Pg.165]

Review articles are indicated by the words Review(s) or Book(s) in hold-faced type. [Pg.165]

3 Classification of chiral dendritic molecules is treated in the Review C. W. Thomas, Y. Tor, Chirality 1998, 10, 53-59. [Pg.165]

8 All known compounds of this kind are derived from l,l -binaphthyl derivatives  [Pg.166]


See other pages where Bibliography and Notes for Section 4.2 Chiral Dendrimers is mentioned: [Pg.165]    [Pg.165]    [Pg.167]   


SEARCH



Bibliography and Notes

Chiral dendrimer

Chiral dendrimers

© 2024 chempedia.info