Hydrolysis of crown ether acetals. Effects of ring size and cation binding

1991 ◽  
Vol 56 (2) ◽  
pp. 673-677 ◽  
Author(s):  
Takumi Oshima ◽  
Toshikazu Nagai
2008 ◽  
Vol 47 (3) ◽  
pp. 1218-1223 ◽  
Author(s):  
Mei-Jin Li ◽  
Zuofeng Chen ◽  
Nianyong Zhu ◽  
Vivian Wing-Wah Yam ◽  
Yanbing Zu
Keyword(s):  

1995 ◽  
Vol 31 (6) ◽  
pp. 559-563 ◽  
Author(s):  
Masamitsu Shirai ◽  
Yoshiki Matoba ◽  
Masahiro Tsunooka

1989 ◽  
Vol 54 (6) ◽  
pp. 1465-1468 ◽  
Author(s):  
Takumi Oshima ◽  
Toshikazu Nagai
Keyword(s):  

2008 ◽  
Vol 63 (9) ◽  
pp. 1101-1106
Author(s):  
Adelė Jonušaite ◽  
Arnold Adam

[Cs(18-crown-6)(CH3CO3)] (1) has been obtained by the reaction of CsOCH3 with 18-crown-6 (1,4,7,10,13,16-hexaoxacyclooctadecane) in methanol in a CO2 atmosphere. The compound crystallizes in the monoclinic space group P21/n (no. 14) with a = 12.141(3), b = 8.610(1), c = 17.985(4) Å , β = 91.17(2)° and V = 1879.6(7) Å3. Cs is tenfold coordinated by six oxygen atoms of the crown ether and four oxygen atoms of two methyl carbonate anions which act as bidentate ligands. The slow hydrolysis of the methylcarbonate results in the hydrogencarbonate complex {Cs2(18-crown- 6)2 · [H2(CO3)2] · H2O · CH3OH} (2), the basic structural constitution of the starting material being retained. This new compound crystallizes in the monoclinic space group P21/c with a = 8.657 (7), b = 22.601 (2), c = 19.619 (15) Å, β = 92.09 (6)° and V = 3836.5 (6) Å3.


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