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Ethylene Evolution From 2-Chloroethylphosphonic Acid
Author(s) -
Shang Fa Yang
Publication year - 1969
Publication title -
plant physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.554
H-Index - 312
eISSN - 1532-2548
pISSN - 0032-0889
DOI - 10.1104/pp.44.8.1203
Subject(s) - ethylene , chemistry , nucleophile , alkene , yield (engineering) , phosphonate , chlorine , molecule , medicinal chemistry , organic chemistry , catalysis , materials science , metallurgy
2-Chloroethylphosphonic acid (CEPA. "Amchem 66-329", "Ethrel"; ref. 1), a new plant growth regulator, degrades to yield ethylene in an alkaline solution. When applied to plants, it has been very effective in causing responses characteristic of ethylene treatment (3, 4, 6, 7). The formation of ethvlene or its alkene homologs from CEPA or its homologs was studied and deFcribed in detail in 1963 by Maynard and Swan (5) including the probable reaction mechanism. Nevertheless, several reports have since appeared describing the same reaction wi.thout citing (4, 8) or properly acknowledging (3) their work. Some investigators (7) have since suggested that the growth regulatory action of CEPA is due to the stimulation of ethylene production within the plant tissues without discussing the fact that CEPA itself is the ethylene producer. The chemical mechanism of ethylene production from CEPA suggested by Maynard and Swan (5) involves the nucleophilic attack on -the phosphonate dianion by a water molecule and the concerted elimination of chlorine, leading to direct formation of phosphate and chloride as shown in equation (I). Probably the OH-ion may also serve as an nucleophile in the reaction.

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