Schatz J, Schildbach F, Lentz A, Rastätter S, Debaerdemaeker T (2001)
Publication Type: Journal article, Original article
Publication year: 2001
Original Authors: Schatz J., Schildbach F., Lentz A., Rastätter S., Debaerdemaeker T.
Publisher: Oldenbourg Verlag
Book Volume: 216
Pages Range: 182-186
Journal Issue: 3
DOI: 10.1524/zkri.216.3.182.20323
The crystal structure of the p-tert-butylcalix[8]arene-chloroform 1:8 clathrate (CHO· 8 CHCl: P1̄, α = 13.886(2) Å, b = 21.891(4) Å, c = 21.930(4) Å, α = 64.00(2)°, β = 78.97(2)°, γ = 88.75(2)°, Z = 2) features a strong CH/π interaction of one chloroform molecule with the π system of one phenol ring of the calix[8]arene moiety; the seven other chloroform molecules occupy interstitial places in the crystal lattice of a highly solvated macrocyclic system (c = 0.566 mol dm). A thermogravimetric analysis also shows that one solvent molecule is bound more tightly than the others. The observed binding motif is presumably based on a subtle interplay between favourable interactions (CH/π and to some extent Cl/π) and induced fit between host and guest.
APA:
Schatz, J., Schildbach, F., Lentz, A., Rastätter, S., & Debaerdemaeker, T. (2001). A ch/π interaction at a highly solvated macrocycle in the solid state - The p-tert-butylcalix[8]arene-chloroform 1:8 clathrate. Zeitschrift für Kristallographie, 216(3), 182-186. https://dx.doi.org/10.1524/zkri.216.3.182.20323
MLA:
Schatz, Jürgen, et al. "A ch/π interaction at a highly solvated macrocycle in the solid state - The p-tert-butylcalix[8]arene-chloroform 1:8 clathrate." Zeitschrift für Kristallographie 216.3 (2001): 182-186.
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