Caged boron-nitrogen compounds containing ester substitution
Abstract
Abstract CAGED BORON-NITROGEN COMPOUNDS HAVING THE FORMULA: (-O-(CXR2X)-N(-(CYR2Y)-O(-))-(CZR2Z)-O-)>B(-) WHERE O AND B ARE JOINED CERTAIN OF THE COMPOUNDS OF THIS INVENTION CONTAIN AT LEAST ONE RING SUBSTITUENT WHEREAS WITH OTHERS AT LEAST TWO OF THE RINGS OF THE COMPOUNDS ARE SUBSTITUTED, WITH AT LEAST ONE OF THE RINGS BEING SUBSTITUTED WITH A HYDROXYALKYL, AMINOALKYL, ARYLALKYL, ARYL, ESTER, AMIDO OR ETHER RADICAL, AND AT LEAST ONE OF THE REMAINING RINGS BEING SUBSTITUTED WITH ONE OF THESE RADICALS OR AN ALKYL RADICAL, BUT ONE RING NEED BE SUBSTITUTED WHEN THE SUBSTITUENT IS A HIGHER C8-C22 ALKYL RADICAL, A HYDROXYL GROUP, A HIGHER C8-C22 ETHER OR ESTER, OR AN ALKYL HIGHER (C8-C22) ETHER OR ESTER. EXEMPLARY OF THESE COMPOUNDS ARE 3,7,10-TRIHYDROXYMETHYL-2, 8,9-TROXA - 5 - AZA - 1 - BORATRICYCLO(3.3.3.0)UNDECANE; 3MEHTYL-7,10-DIPHENYL-2,8,9-TRIOXA-5-AZA - 1 - BORATRICYCLO (3.3.3.0)UNDECANE; AND 3-HYDROXYMETHYL-7,10-DIMETHYL-2, 8,9-TRIOXA-5-AZA-1-BORATRICYCLO(3.3.3.0)UNDECANE STEARATE. THE COMPOUNDS ARE USEFUL AS ANTISTATIC AGENTS IN NATURAL AND SYNTHETIC, POLYMERIC FIBERS AND FILMS, AND AS COLOR IMPROVING AGENTS FOR FATTY ACID DISTILLATIONS.
Inventors
- 👤 J Ludwig
- 👤 K Witsken
Bibliographic Details
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