81536-01-8Relevant academic research and scientific papers
CALIXARENES 9 CONFORMATIONAL ISOMERS OF THE ETHERS AND ESTERS OF CALIXARENES
Gutsche, C. David,Dhawan, Balram,Levine, Jeffrey A.,No, Kwang Hyun,Bauer, Lorenz J.
, p. 409 - 426 (2007/10/02)
Calixarene (1A), p-t-butylcalixarene (1B), and p-allylcalixarene (1C) have been converted to various derivatives, including the methyl, ethyl, allyl, benzyl and trimethylsilyl ethers and the acetates.Although the parent calixarenes exist preferentially in the cone conformation, they are conformationally flexible and at room temperature interconvert at a rate of ca 100 sec-1.All but the methyl ethers, on the other hand, are conformationally rigid at the room temperature.The preferred conformations in most cases are the cone and the partial cone, depending on the derivative formed (i.e. methyl and ethyl ethers favour the partial cone; benzyl and trimethylsilyl ethers favour the cone).In the cases of the allyl ethers and the acetates the p-substituents appear to influence the conformational outcome (i.e. 1A and 1B form the allyl ethers in the partial cone and cone conformation, respectively; 1A and 1B form the acatates in the 1,3-alternate and partial cone conformation, respectively).The conformationally rigid calixarene derivatives in the cone and partial cone conformations belong to the small group of synthetic compounds that contain a permanent cavity (a "changeless calix") whose dimensions are large enough to encapsulate other molecules.
Calixarenes. 8. Short, Stepwise Synthesis of p-Phenylcalixarene, p-Phenyl-p-tert-butylcalixarene, and Derived Products
No, Kwang Hyun,Gutsche, C. David
, p. 2713 - 2719 (2007/10/02)
Calixarenes (Schemes I-IV) have been previously obtained by a one-flask process (Zinke synthesis) and by a multistep process (Hayes and Hunter synthesis).The former has the advantage of speed and simplicity but the disadvantage of difficult-to-separate pr
