ABSTRACT
E. GIGINEISHVILI, L. ASATIANI, N. LEKISHVILI, A. D’AMORE, and G. E. ZAIKOV
17.1 Introduction .................................................................................. 284 17.2 Experimental ................................................................................ 284
17.2.1 1-ferrocenyl-1-phenyl-1-oxy-2-pentyn-4-en-FK-1G (I) ... 285 17.2.2 1,1I-bis(-1-phenyl-1-oxy-2-pentyn-4-enyl)
ferrocene-FK-2G (II) ....................................................... 285 17.2.3 1-ferrocenyl-1-phenyl-1-metoxy-2-pentyn-4-en (III) ....... 285 17.2.4 1,1I-bis (1-phenyl-1-metoxy-2-pentyn-4-enyl
ferrocene (IV) ................................................................... 286 17.2.5 1-ferrocenil-1-phenyl-1,4-pentadien-3-one (V) ................ 286 17.2.6 1,1I-bis(1-phenyl-1,4-pentadien-3-on)ferrocene (VII)
and 1,3-bis-phenyl-1,3-bis(vinyl-ethinyl)-2-oxa [3]-ferrocenophane (VIII) ................................................. 286
17.3 General Results ............................................................................ 287 17.4 Use Of Synthesized Ferocenecontaining Alcohols ...................... 298 17.5 Conclusions .................................................................................. 299 Keywords .............................................................................................. 300 References ............................................................................................. 300
17.1 INTRODUCTION
It is known from literature that some derivatives of ferrocene and ferrocene-containing carbinoles as catalysts of special purpose for burning of solid fuel [1] have found a wide application. Possessing such properties as thermal stability, low toxicity, good solubility in organic solvents producing nearly smokeless burning of organic compounds, they are valuable additives to all fuels (gas, liquid, solid).
