Buy article online - an online subscription or single-article purchase is required to access this article.
Download citation
Download citation
link to html
The high symmetry and round shape of the fullerene molecules induce orientational phenomena that play an important role in the properties of the fullerene compounds. This is illustrated in this review which is focused on the orientational properties of C60 monomer and polymer structures. First, the orientational state of C60 at room temperature, its peculiar orientational ordering phase transition and the associated glassy state are described, together with the corresponding temperature-pressure phase diagram. Then, a summary of the polymerization processes and of the varied structures obtained under high-pressure high-temperature conditions or via doping by alkali metals is proposed. Finally, some information is given on the orientational properties of C60 layers and surfaces.

Subscribe to Acta Crystallographica Section A: Foundations and Advances

The full text of this article is available to subscribers to the journal.

If you have already registered and are using a computer listed in your registration details, please email support@iucr.org for assistance.

Buy online

You may purchase this article in PDF and/or HTML formats. For purchasers in the European Community who do not have a VAT number, VAT will be added at the local rate. Payments to the IUCr are handled by WorldPay, who will accept payment by credit card in several currencies. To purchase the article, please complete the form below (fields marked * are required), and then click on `Continue'.
E-mail address* 
Repeat e-mail address* 
(for error checking) 

Format*   PDF (US $40)
   HTML (US $40)
   PDF+HTML (US $50)
In order for VAT to be shown for your country javascript needs to be enabled.

VAT number 
(non-UK EC countries only) 
Country* 
 

Terms and conditions of use
Contact us

Follow Acta Cryst. A
Sign up for e-alerts
Follow Acta Cryst. on Twitter
Follow us on facebook
Sign up for RSS feeds