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Chelating P2-Bis-phosphazenes with a (R, R)-1, 2- Diaminocyclohexane Skeleton : Two New Chiral Superbases (CROSBI ID 238314)

Prilog u časopisu | izvorni znanstveni rad | međunarodna recenzija

Kogel, Julius F. ; Kovačević, Borislav ; Ullrich, Sebastian ; Xie, Xiulan ; Sundermeyer, Jorg Chelating P2-Bis-phosphazenes with a (R, R)-1, 2- Diaminocyclohexane Skeleton : Two New Chiral Superbases // Chemistry : a European journal, 23 (2017), 11; 2591-2598. doi: 10.1002/chem.201604522

Podaci o odgovornosti

Kogel, Julius F. ; Kovačević, Borislav ; Ullrich, Sebastian ; Xie, Xiulan ; Sundermeyer, Jorg

engleski

Chelating P2-Bis-phosphazenes with a (R, R)-1, 2- Diaminocyclohexane Skeleton : Two New Chiral Superbases

The linkage of two P2-phosphazenyl groups through a C2-symmetric (R, R)-1, 2-diaminocyclohexane (DACH) backbone yielded the new chiral superbases DACHP2NMe2 and DACH-P2Pyr (Pyr=pyrrolidinyl). These bases were prepared by a Kirsanov reaction and studied with respect to their spectroscopic and structural characteristics. Theoretical calculations concerning their basicity properties revealed remarkable pKBH + values of 38.1 and 39.9 on the acetonitrile scale ; this makes them the strongest nonionic chiral superbases known to date.

basicity ; chirality ; density functional calculations ; phosphazenes ; superbases

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Podaci o izdanju

23 (11)

2017.

2591-2598

objavljeno

0947-6539

10.1002/chem.201604522

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Kemija

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