FEDERAL INSTITUTE OF INDUSTRIAL PROPERTY RU proposal Date: 15.02.2016 Project : D 25 Subclass : C 07F Re. : IPC/WG/5/3 par. 23 Classification definitions for subclass C 07F 1. Title ACYCLIC, CARBOCYCLIC, OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM, OR TELLURIUM 2. Definition statement This subclass covers: A. Organic (acyclic, carbocyclic, heterocyclic) compounds containing elements other than carbon, hydrogen, halogen, oxygen, nitrogen, sulfur, selenium, or tellurium with or without them (e.g. metallo-organic compounds, boron compounds, silicon compounds, phosphorus compounds, arsenic compounds). B. The preparation of compounds under the subclass definition including purification, separation, stabilisation or use of additives (see Class C07, 1 note) unless provided for elsewhere, as specified below. C. The treatment and modification of compounds under the subclass definition (except for mechanical treatment) provided that (1) the treatment is not provided for elsewhere and (2) the resultant product is a compound under the subclass definition. 3. Relationships between large subject matter areas This subclass is a functional-oriented entry, thus, it does not cover the application or use of the compounds under the subclass definition. For classifying such information other entries in IPC exist, e.g: A 01 N PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES, AS HERBICIDES REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS PEST A 61 K PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES 4. Limiting references 1. Products obtained from layered base-exchange silicates by ion-exchange with organic compounds such as ammonium, phosphonium or sulfonium compounds or by intercalation of organic compounds C01B 33/44. 2. Metal-containing porphyrins C07D 487/22. 3. Sugar phosphates C07H 11/04. 4. Nucleotides C07H 19/00, 21/00. 5. Nucleic acids C07H 21/00. 6. Macromolecular compounds C08. 7. Organic acid salts, alcoholates, phenates, chelates or mercaptides, having no elements other than carbon, hydrogen, halogen, oxygen, nitrogen, sulfur, selenium, or tellurium in the parent compounds C07C, C07D (attention is drawn to note 5 following the title of class C07 concerning the rules of classification of these compouns). 8. Fermentation or enzyme-using processes to synthesise a desired chemical compound or composition or to separate optical isomers from a racemic mixture C12P. 9. Production of organic compounds by electrolysis or electrophoresis C25B 3/00, 7/00 5. Informative references 1. Dyes C09. 2. Fermentation products C12. 6. Special rules of classification 1. The last place rule in whole Class C07 (See Class C07, 2 note) is also effective for this subclass. According to it, e.g. sugar phosphates are classified in group C07H 11/04 as sugars and not in group C07F 9/00 as phosphorus compounds (See also Limiting References 2, 3, 4) and peptides are classified in subclass C07K. 2. In this subclass, in the absence of an indication to the contrary, classification is made in the last appropriate place, e.g. ferrocenes and cobaltocenes are classified in in group C07F 17/00 and not in group C07F 15/00 (See Class C07, 2 note) 3. Metal compounds according to more than one of main groups C07F 1/00 – 17/00 are classified in group C07F 19/00. 4. In this subclass, organic acid salts, alcoholates, phenates, chelates or mercaptides are classified as the parent compounds (See subclass C07F, 3 note). 5. Salts, adducts or complexes formed between two or more organic compounds are classified according to all compounds forming the salts, adducts or complexes (See Class C07, 5 note). 6. Therapeutic activity of compounds is further classified in subclass A61P. 7. In this subclass it is desirable to add indexing codes of subclass C07M. The indexing codes should be unlinked. 7. Glossary of terms 1. Metallocene – dicyclopentadienyl compound of transitional metal, e.g., ferrocenes. 2. Salt – product of substitution of hydrogen in carboxyl group of acid by ion of metal or other cation. 3. Phenate – product of substitution of hydrogen in hydroxy group of phenol by metal atom. 4. Alcoholate - product of substitution of hydrogen in hydroxy group of alcohole by metal atom. 5. Chelate – intracomplex compound i.e. compound containing intramolecular donoracceptor bonds. 6. Metallo-organic compound – organic compound containing Me – C bond. 7. Organic compound – compound characterized by having (a) at least two carbon atoms bonded together or (b) one carbon atom bonded to at least one atom of hydrogen, halogen or nitrogen, except for hydrogen cyanide, cyanogen, cyanamide, cyanogen halide, carbides, phosgene, thiophosgene, cyanic, thiocyanic, isocyanic, isothiocyanic, carbamic acids. 8. Synonyms and keywords 1. Cyclopentadienyl – (chemical formulae) 2. Indenyl – (chemical formulae) 3. Fluorenyl - (chemical formulae) 4. Silane – compound having chemical formulae SinH2n+2. (Organic derivatives of silane are, e.g., methylmonosilane CH3SiH3, dimethyldichlorosilane Si(CH3)2CL2, hexamethyldisilane (CH3)3Si – Si(CH3)3) 5. Siloxane – organic silicon compound containing Si – O – Si bonds. 6. Silicononane – tetraethylsilane 7. Silanole - organic silicon compound containing Si – OH bonds, e.g. trimethylsilanole (CH3)3SiOH, dimethylsilanediole (CH3)2SiOH. 8. Silasane - organic silicon compound containing Si – NH – Si bonds. 9. Siltiane - organic silicon compound containing Si – S – Si bonds. 10. Silamine - organic silicon compound containing R – SiH2 – NH2 bonds. 11. Phosphine - compound having chemical formulae PnHn+2 or Pn (Organic derivative of phosphine is, e.g., dimethylphosphine (CH3)2PH) 12. Arsine - compound having chemical formulae AsnHn+2. (Organic derivative of arsenic is, e.g., dichloromethylarsine CH3AsCl2, dimethyldichlorodiarsine (CH3)2As –AsCL2). 13. Cacodyl – tetramethyldiarsine (CH3)2As –As(CH3)2. 14. Cacodylic acid - compound having chemical formulae (CH3)2AsOOH. 15. Stibine - compound having chemical formulae SbnHn+2. (Organic derivative of antimony is, e.g., trimethylstibine Sb(CH3)3). M. Sobolev