The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Aug. 11, 1987

Filed:

Feb. 25, 1986
Applicant:
Inventors:

Tuong Huynh-Ba, Pully, CH;

Maged A Osman, Zurich, CH;

Attorney:
Primary Examiner:
Int. Cl.
CPC ...
C09K / ; C07D / ; C07C / ; C07C / ; C07C / ; C07C / ; C07C / ;
U.S. Cl.
CPC ...
544224 ; 25229961 ; 25229962 ; 25229963 ; 544238 ; 544239 ; 558388 ; 558398 ; 558406 ; 558410 ; 558389 ; 558399 ; 558409 ; 558426 ; 558428 ; 558429 ; 558430 ; 560-1 ; 560 55 ; 560 64 ; 560 66 ; 560 73 ; 560105 ; 560108 ; 560116 ; 560-8 ; 560 59 ; 560 65 ; 560 72 ; 560102 ; 560107 ; 560118 ; 560126 ; 560138 ; 560141 ; 568631 ; 568632 ; 568634 ; 568642 ; 568659 ; 568661 ; 568664 ; 568665 ; 570129 ; 570130 ; 570182 ; 570183 ; 570184 ; 570185 ; 570187 ; 570188 ;
Abstract

New anisotropic compounds with a cross-polarizing substituent have the formula (1) ##STR1## The increase in .epsilon..perp. is achieved by the polarizing group X, preferably the cyano group or a halogen atom, which is not laterally on the ring, as with the known compounds, but is on the bridge, that is to say is part of the main bridge bonding rings A and B to one another. Ring A has the formula (1a) or (1b) given herein and is always cycloaliphatic, while ring B can be identical to ring A or is an aromatic ring of the formula (1c) or (1d) herein. R.sup.1 and R.sup.2 are identical or different end groups of the formula (1e) herein. The radical X on the bridge causes less widening of the molecule than a radical X on a ring, which provides comparatively higher clear points and moreover enables aromatic rings to be omitted from the anisotropic compounds.


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