The diamond phase precursor, viz., poly(naphthalenehydrocarbyne) (1), was prepared. Its disordered structure is built of CH fragments with sp 3 hybridized carbon atoms, and arene fragments are inserted in the structure. The use of 1 in the process of diamond layer deposition makes it possible to prepare highly qualitative thin diamond coatings with low roughness and good optical properties.Uniform thin diamond films (DFs) with low surface roughness and nanocrystalline internal structure are de manded for planar electronic devices, protective optical coatings, and micro and nanoelectromechanical sys tems. 2 The most important condition for preparation of such DFs is efficient nucleation, for which the method with ultradispersed diamond (UDD) deposition (usual for thick (>1 μm) 3 DFs) is inappropriate because of low den sity and nonuniform nuclei distribution on the substrate. It is known that the efficiency of UDD application can be enhanced by deposition of a layer of carbon 4 and ceramics SiC, SiN x , and TiSiN (see Ref. 5). However, nuclei gener ation from an appropriate precursor can serve as a radical method for nucleation improvement. Poly(phenylcarbyne) has been used earlier 6-9 for this purpose. However, thus obtained films consisted of diamond like carbon with dia mond inclusions. In the present study, we describe the synthesis of poly(naphthalenehydrocarbyne) (1), viz., a new precursor combining the aliphatic framework and aromatic fragments in its structure. Its structure and po tential for using in diamond layer deposition on a silicon substrate were studied.
Results and DiscussionSynthesis of polymer 1. The general method for pre paration of polymers of the poly[(R )carbyne] series (R = Ar, Alk, H), in particular, polymers 2 and 3, is the condensation of heme trihalides by the action of a KNa alloy in the ultrasonic field 10,11 (Scheme 1, reaction a) or by electrolysis 12,13 (Scheme 1, reaction b). Note that these methods have several substantial drawbacks. For exam ple, the use of an explosive KNa alloy in reaction a makes the latter almost impracticable. Reaction b is also very difficult in methodical respect (anaerobic electrolysis ac companied by Cl 2 evolution is required, the product needs purification by prolonged heating with LiAlH 4 , etc. 12,13 ). The product yield in procedures a and b is low, and a strong dependence of the properties of the polymers on many random factors is observed. Thus, search for convenient methods of synthesis of poly(carbynes) and, first of all, poly(hydrocarbyne) (3) as the most promising of them, remains topical. Scheme 1 a. Ultrasonication. b. Electrolysis. R = Ph (2), H (3)