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- W2023961569 abstract "The p-iodotetrafluorophenyl motif has been appended to the four alcoholic groups of pentaerythritol to give the corresponding tetraether 1, which works as an effective tecton in halogen bonding based crystal engineering. In fact, in the solution and the solid phases, the halogen bonding drives the self-assembly of this ether with primary, secondary, and tertiary amines as well as with pyridine derivatives. Co-crystals are isolated where 1 invariably works as a tetradentate halogen bonding donor. Double strand, 1D, infinite chains are formed where the nitrogen substituted motifs are pinned in positions that fulfil Schmidt's requirements for solid phase photocycloaddition reactions. Quantitative yields and complete stereoselectivity have been obtained in the cycloaddition reaction." @default.
- W2023961569 created "2016-06-24" @default.
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- W2023961569 creator A5014263754 @default.
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- W2023961569 creator A5043992055 @default.
- W2023961569 creator A5060310701 @default.
- W2023961569 creator A5081562507 @default.
- W2023961569 date "2005-02-01" @default.
- W2023961569 modified "2023-10-18" @default.
- W2023961569 title "Pentaerythritol tetrakis(4-iodo-2,3,5,6-tetrafluorophenyl) ether: a tecton for the self-assembly of double strand 1D infinite chains" @default.
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