31-Benz­yloxy-5,11,17,23,29-penta-tert-butyl­calix[5]arene-32,33,34,35-tetra­ol

نویسندگان

  • Claudia Gargiulli
  • Giuseppe Gattuso
  • Anna Notti
  • Francesco Nicoló
  • Andrea Pappalardo
چکیده

The title compound, C62H76O5, known to be one of the most versatile synthetic precursors/inter-mediates of calix[5]arene derivatives, adopts an approximate Cs -symmetric cone-in conformation. The aryl-oxybenzyl ring is tilted in such a way that the p-tert-butyl group fills the macrocycle cavity, while the benzyl group moves away from the cavity axis. In the crystal, this conformational arrangement is secured by intra- and inter-molecular O-H⋯O hydrogen bonds forming inversion dimers. Four tert-butyl groups are disordered over two orientations, with occupancy ratios of 0.745 (6):0.255 (6), 0.837 (5):0.163 (5), 0.850 (5):0.150 (5) and 0.845 (8):0.155 (8).

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

5,11,17,23,29-Penta-tert-butyl-31,32,33,34,35-penta­propoxycalix[5]arene dichloro­methane hemisolvate

The title compound, tert-butyl-propoxycalix[5]arene, C(70)H(100)O(5)·0.5CH(2)Cl(2), crystallizes as a solvate with two mol-ecules of calix[5]arene in 1,2-alternate conformations and one mol-ecule of dichloro-methane in the asymmetric unit. One tert-butyl group in one of the mol-ecules and two in the other are disordered over two positions with occupancy factors fixed at 0.5917:0.4083, 0.5901:0....

متن کامل

25,26,27,28-Tetra­butoxy-5,11,17,23-tetra-tert-butyl­calix[4]arene chloro­form tetra­solvate dihydrate

The title compound, C(60)H(88)O(4)·4CHCl(3)·2H(2)O, is the alkyl-ated product of 5,11,17,23-tetra-tert-butyl-calix[4]arene. It adopts a distorted cone conformation which leads to an open cavity. All the phenolic rings are tilted so that their tert-butyl groups are pitched away from the calix cavity. Two opposite aromatic rings are close to being perpendicular to one another [dihedral angle 85.0...

متن کامل

Alkali metal ion select ability of di-propoxy- p-tert-butyl-Calix[4]arene, synthesized in acetonitrile

Synthesis and cation selectivity of 25, 27, dipropoxy-26, 28, Di-propoxy 5, 11, 17, 23, ptert-butyl Calix[4]arene are studied in acetonitrile solution. The stability constants of differentcomplexes of Calixarene (as a ligand) with alkali metal cations are determined at 25 °C by usingspectrophotometric technique.On the basis of calculations, complexation of Calixarene with Cs+and Li+ are more fa...

متن کامل

Selective Oxidation of 25,27-Bis- (3-formylphenoxylethoxy)-p-tert-butylcalix[4]arene

Reaction of 25,27-bis-(3-formylphenoxyethoxy)-p-tert-butylcalix[4]arene (1) with 20% mole of KCN in ethanol and i-propanol yielded monoethylester (2) (50%) and monoisopropylester (3) (15%). Compound 1 was not oxidized by air in the absence of KCN under reflux. The Cannizzaro reaction of 1 in ethanol using KOH gave bis-alcohol (4), acid-alcohol (5).

متن کامل

Ethyleneglycol tungsten complexes of calix[6 and 8]arenes: synthesis, characterization and ROP of ε-caprolactone.

By varying the reaction conditions, the reaction of [W(eg)3] (eg = 1,2-ethanediolato) with p-tert-butylcalix[n]areneHn (n = 6 or 8) in refluxing toluene affords, following work-up, a number of products which have been fully characterized. From the reaction of p-tert-butylcalix[6]areneH6 with one or two equivalents of [W(eg)3], only the oxo-bridged complex {[W(eg)]2(μ-O)p-tert-butylcalix[6]arene...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:

دوره 68  شماره 

صفحات  -

تاریخ انتشار 2012