Stereochemistry of Molecules in Crystals (part 1, 2)

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Br · ax host Br host 659 <strong>in</strong>clusion compound 687 790 770 750 730 710 690 wavenumber (cm -1 ) 670 Fig. IR spectra with us<strong>in</strong>g the ATR.
· ax Cl I (cps) host 2 θ · ax Br host I (cps) 2 θ Fig . X-ray powder diffraction pattern Chem. Comm. 2005, 3646.
Page 1 and 2: Stereochemistry of Molecules in Cry
Page 3 and 4: 1) acetylacetone-enol form part 1:
Page 5 and 6: 2) acylic acid-monomeric s-trans fo
Page 7 and 8: H O H O OH Ph 2 C CPh 2 OH s-trans
Page 9 and 10: Ph 2 C OH (R, R)-(-)- O O H H · O
Page 11 and 12: H H θ = 5(4) º Cl CH 3 H H
Page 13 and 14: 5) halocyclohexane - eq X X eq ax a
Page 15 and 16: F F Cl F F Fig. X-ray structure of
Page 17 and 18: F F rac - O O OH OH · eq Br F host
Page 19 and 20: · ax Cl host Fig. Packing diagram
Page 21: Cl 1,3-diaxial interaction (hydroge
Page 25 and 26: 8) enantiomerization Ph tBu C OH N
Page 27 and 28: 2) photochromism O Ph Zn-ZnCl 2 O P
Page 29 and 30: 4) succinamide, generation of chila

Stereochemistry of Molecules in Crystals (part 1, 2)

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