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:
Jun. 24, 2025

Filed:

Jan. 26, 2022
Applicant:

Countertrace, Llc, Manvel, TX (US);

Inventors:

Robert E. Hanes, Jr., Missouri City, TX (US);

Richard L. Pettys, Pearland, TX (US);

David M. Headley, Pearland, TX (US);

Paul T. Hoopingarner, Missouri City, TX (US);

Assignee:

COUNTERTRACE, LLC, Manvel, TX (US);

Attorney:
Primary Examiner:
Assistant Examiner:
Int. Cl.
CPC ...
C07C 22/04 (2006.01); C07C 235/60 (2006.01); C07C 247/10 (2006.01); C07D 249/06 (2006.01); C07D 303/36 (2006.01); C07D 405/14 (2006.01);
U.S. Cl.
CPC ...
C07C 22/04 (2013.01); C07C 235/60 (2013.01); C07C 247/10 (2013.01); C07D 249/06 (2013.01); C07D 303/36 (2013.01); C07D 405/14 (2013.01);
Abstract

Phenyl rings provide a robust scaffold for molecular design, given the limited number of ring carbon atoms and the fixed geometry in between. However, it can be difficult to form highly substituted phenyl rings suitable for covalent attachment of multiple moieties thereto. Moreover, binding phenyl rings to a surface in a fixed geometry may be difficult. Hexasubstituted benzenes having certain structural features may alleviate the foregoing difficulties by providing versatile groups for further functionalization and surface attachment. Such hexasubstituted benzenes may have a structure of in which each X is independently Cl, Br or N, and each Z is independently —CH(Br)CH, —CH(N)CH, —CH═CH, —CHCH, —CHCHSiR'(R′=hydrocarbyl), or Alternating groups in the hexasubstituted benzenes may be directed toward opposite faces of the phenyl ring, such that orthogonal reactive groups are directed toward the opposite faces. Certain groups may facilitate surface attachment of the hexasubstituted benzenes.


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