Aristotle University Of Thessaloniki (AUTH)
ΣΥΝΘΕΣΗ ΚΑΙ ΧΗΜΕΙΟΦΩΤΑΥΓΕΙΑ ΔΙΥΠΟΚΑΤΕΣΤΗΜΕΝΩΝ ΣΤΙΛΒΕΝΙΩΝ
Abstract
dc:descriptionTHE SYNTHESIS OF A SERIES OF E-2-HYDROXY-4'-SUBSTITUTED STILBENES WAS ACCOMPLISHED IN GOOD YIELDS BY THE WITTIG CARBONYL OLEFINATION REACTION. THE OZONOLYSIS OF THESE STILBENOLS WAS FOUND TO BE CHEMILUMINESCENT, THE QUANTUM YIELDS (1,2X10-4 - 8,1X10-6) DEPENDING ON HAMMETT'S "6" CONSTANT FOR THE 4'- SUBSTITUENT, AND SALICYLALDEHYDE ANION WAS FOUND TO BE THE PRIMARY EMOITLER IN ALL CASES. THE REACTION OF THE SAME STIBENOLS WITH SINGLET OXYGEN WAS ALSO CHEMILUMINESCENT WITH QUANTUM YIELDS 1,5X10-5 - 5,0X10-8. THE REACTION DOES NOT GO THROUGH A 1,2 DIOXETANE INTERMEDIATE AND THE MOLECULE EMITTING LIGHT IS FOUND TO BE STILBENOL ITSELF, PROBABLY VIA A C.I.E.E.L MECHANISM. FURTHERMORE WITTIG REACTIONS OF SEMISTABILIZED YLIDES WERE STUDIED FROM A MECHANISTIC POINT OF VIEW. DIFFERENCES IN STEREOSELECTIVITY BETWEEN THE TWO SERIES OF REACTIONS WERE RATIONALIZED IN TERMS OF STERIC RATHER THAN ELECTRONIC FACTORS. OXAPHOSPHETANES WHICH MAY COLLAPSE TO OLEFINS OR DECOMPOSE TO LI+ -STABILIZED BETAINE COMPLEXES ARE POSTULATED AS THE IMPORTANT INTERMEDIATES.
Degree
thesis:*- Grantor dc:publisher
- Aristotle University Of Thessaloniki (AUTH)
- Year dc:date
- 1988
Author and committee
dc:creator, dc:contributor.*- Author dc:creator
-
- Μυλωνά, Αναστασία
Subjects
dc:subject × 13Rights
- Language dc:language
- gre
Identifiers
dc:identifier.*- Identifier
- 10.12681/eadd/0716
- OAI identifier oai:identifier
- oai:10442/0716