TY - JOUR
T1 - Reactions of alkoxyl derivatives of a layered perovskite with alcohols
T2 - Substitution reactions on the interlayer surface of a layered perovskite
AU - Suzuki, Hiromi
AU - Notsu, Kazuya
AU - Takeda, Yosuke
AU - Sugimoto, Wataru
AU - Sugahara, Yoshiyuki
PY - 2003/2/11
Y1 - 2003/2/11
N2 - Organic derivatives of a layered perovskite compound, HLaNb2O7·xH2O (HLN), with interlayer surfaces possessing n-alkoxyl groups (n-decoxyl and n-propoxyl) have been allowed to react with various alcohols and a diol (ethylene glycol) to form new organic derivatives via substitution reactions. The reaction of an n-propoxyl derivative of HLN with n-decanol leads to the formation of n-decoxyl groups bound to the interlayer surface of the perovskitelike [LaNb2O7] slab. In a similar fashion, the reaction of an n-decoxyl derivative of HLN with 2-propanol results in the formation of an isopropoxyl derivative. The reaction of the n-decoxyl derivative of HLN with tert-butyl alcohol also proceeds, though the reaction is not completed even after 14 days. After the reaction of the n-decoxyl derivative of HLN with ethylene glycol, only one of the two hydroxyl groups in ethylene glycol is reacted, and -OCH2CH2OH groups are present on the interlayer surface. Water is required for proceeding the substitution reaction between the n-propoxyl derivative of HLN and n-decanol, and the reaction mechanism involving hydrolysis of the alkoxyl groups on the interlayer surface and subsequent esterification is proposed.
AB - Organic derivatives of a layered perovskite compound, HLaNb2O7·xH2O (HLN), with interlayer surfaces possessing n-alkoxyl groups (n-decoxyl and n-propoxyl) have been allowed to react with various alcohols and a diol (ethylene glycol) to form new organic derivatives via substitution reactions. The reaction of an n-propoxyl derivative of HLN with n-decanol leads to the formation of n-decoxyl groups bound to the interlayer surface of the perovskitelike [LaNb2O7] slab. In a similar fashion, the reaction of an n-decoxyl derivative of HLN with 2-propanol results in the formation of an isopropoxyl derivative. The reaction of the n-decoxyl derivative of HLN with tert-butyl alcohol also proceeds, though the reaction is not completed even after 14 days. After the reaction of the n-decoxyl derivative of HLN with ethylene glycol, only one of the two hydroxyl groups in ethylene glycol is reacted, and -OCH2CH2OH groups are present on the interlayer surface. Water is required for proceeding the substitution reaction between the n-propoxyl derivative of HLN and n-decanol, and the reaction mechanism involving hydrolysis of the alkoxyl groups on the interlayer surface and subsequent esterification is proposed.
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U2 - 10.1021/cm0200902
DO - 10.1021/cm0200902
M3 - Article
AN - SCOPUS:0037431966
SN - 0897-4756
VL - 15
SP - 636
EP - 641
JO - Chemistry of Materials
JF - Chemistry of Materials
IS - 3
ER -