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Influence of structure of cyclic urea derivatives on their reactivities with cotton
Author(s) -
Jung H. Z.,
Benerito R. R.,
Gonzales E. J.,
Berni R. J.
Publication year - 1969
Publication title -
journal of applied polymer science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.575
H-Index - 166
eISSN - 1097-4628
pISSN - 0021-8995
DOI - 10.1002/app.1969.070130914
Subject(s) - chemistry , urea , ring (chemistry) , cellulose , carbonium ion , reaction mechanism , polymer chemistry , catalysis , salt (chemistry) , metal , reaction rate , hydrogen bond , medicinal chemistry , molecule , organic chemistry
The structure of the cyclic urea influenced the rate of reaction with cotton cellulose and the mechanism by which reaction occurred. Reaction of N , N ′‐dimethylolethylene‐urea (DMEU) and N , N ′‐dimethylolpropyleneurea (DMPU) with cellulose in presence of inorganic salt catalysts proceeded through methylol hydroxyls and at the same rate; but reaction mechanism differed. With DMEU, N → metal ion coordination occurred and S N 2 mechanism prevailed. With DMPU, O → metal ion coordination resulted. Reaction of dihydroxyethylene urea (DHEU), N , N ′‐dimethyldihydroxyethyleneurea (DMeDHEU), and N , N ′‐dimethyloldihydroxyethyleneurea (DMDHEU) with cotton cellulose proceeded through ring hydroxyls with the formation of a carbonium ion, indicating an S N 1 mechanism. The much faster rate of reaction with DMeDHEU than with DHEU was attributed to the more electronegative environment of its ring hydroxyl, while the much slower rate of reaction of DMDHEU was attributed to hydrogen bonding between its methylol and ring hydroxyls.