Literature DB >> 16272597

2,6-di-tert-butylphenol revisited at 110 K.

Martin Lutz1, Anthony L Spek.   

Abstract

The title compound, C(14)H(22)O, was studied at 110 K. The phenolic hydroxy group was found to be coplanar with the benzene ring and, due to steric hindrance from the tert-butyl groups, this hydroxy group does not form hydrogen bonds. The shortest intermolecular O...O distance is 3.1008 (11) A, with an O-H...O angle of 117.3 (16) degrees . There are no significant intermolecular pi-pi stacking or C-H...pi interactions.

Entities:  

Year:  2005        PMID： 16272597     DOI： 10.1107/S0108270105030325

Source DB:  PubMed          Journal:  Acta Crystallogr C        ISSN： 0108-2701            Impact factor:   1.172


  2 in total

1.  Sterically shielded pyramidal amino groups in two 4,4'-(arylmethylene)bis(6-allyl-3-chloro-2-methylaniline) derivatives.

Authors:  Maria C Blanco; Alirio Palma; Ali Bahsas; Michael B Hursthouse; Justo Cobo; Christopher Glidewell
Journal:  Acta Crystallogr C       Date:  2009-08-26       Impact factor: 1.172

2.  First hydrogen-bonded adduct of sterically hindered 2-tert-butyl-4-methyl-phenol (TBMP) with 1,3,6,8-tetra-aza-tri-cyclo-[4.4.1.13,8]dodecane (TATD) via coupling of classical hydrogen bonds and C-H⋯π non-covalent inter-actions.

Authors:  Augusto Rivera; Jaime Ríos-Motta; Michael Bolte
Journal:  Acta Crystallogr E Crystallogr Commun       Date:  2022-05-17
  2 in total

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