Kraus et al., 1932 - Google Patents
Aliphatic germanium derivatives. I. Triethylgermanium compounds; some of their properties and reactionsKraus et al., 1932
- Document ID
- 7108465328585763008
- Author
- Kraus C
- Flood E
- Publication year
- Publication venue
- Journal of the American Chemical Society
External Links
Snippet
When three of the valences of the fourth group elements are satisfied by hydrogen or, more frequently, hydrocarbon radicals, they form groups of the type R3A which in many respects resemble corresponding derivatives of carbon. In the case of tin, for example, the tertiary …
- YMSWJBZPRYKQHJ-UHFFFAOYSA-N triethylgermanium data:image/svg+xml;base64,PD94bWwgdmVyc2lvbj0nMS4wJyBlbmNvZGluZz0naXNvLTg4NTktMSc/Pgo8c3ZnIHZlcnNpb249JzEuMScgYmFzZVByb2ZpbGU9J2Z1bGwnCiAgICAgICAgICAgICAgeG1sbnM9J2h0dHA6Ly93d3cudzMub3JnLzIwMDAvc3ZnJwogICAgICAgICAgICAgICAgICAgICAgeG1sbnM6cmRraXQ9J2h0dHA6Ly93d3cucmRraXQub3JnL3htbCcKICAgICAgICAgICAgICAgICAgICAgIHhtbG5zOnhsaW5rPSdodHRwOi8vd3d3LnczLm9yZy8xOTk5L3hsaW5rJwogICAgICAgICAgICAgICAgICB4bWw6c3BhY2U9J3ByZXNlcnZlJwp3aWR0aD0nMzAwcHgnIGhlaWdodD0nMzAwcHgnIHZpZXdCb3g9JzAgMCAzMDAgMzAwJz4KPCEtLSBFTkQgT0YgSEVBREVSIC0tPgo8cmVjdCBzdHlsZT0nb3BhY2l0eToxLjA7ZmlsbDojRkZGRkZGO3N0cm9rZTpub25lJyB3aWR0aD0nMzAwLjAnIGhlaWdodD0nMzAwLjAnIHg9JzAuMCcgeT0nMC4wJz4gPC9yZWN0Pgo8cGF0aCBjbGFzcz0nYm9uZC0wIGF0b20tMCBhdG9tLTEnIGQ9J00gMjg2LjQsMTQzLjUgTCAyMjcuMCwxOTguMScgc3R5bGU9J2ZpbGw6bm9uZTtmaWxsLXJ1bGU6ZXZlbm9kZDtzdHJva2U6IzNCNDE0MztzdHJva2Utd2lkdGg6Mi4wcHg7c3Ryb2tlLWxpbmVjYXA6YnV0dDtzdHJva2UtbGluZWpvaW46bWl0ZXI7c3Ryb2tlLW9wYWNpdHk6MScgLz4KPHBhdGggY2xhc3M9J2JvbmQtMSBhdG9tLTEgYXRvbS0yJyBkPSdNIDIyNy4wLDE5OC4xIEwgMTc1LjgsMTgyLjEnIHN0eWxlPSdmaWxsOm5vbmU7ZmlsbC1ydWxlOmV2ZW5vZGQ7c3Ryb2tlOiMzQjQxNDM7c3Ryb2tlLXdpZHRoOjIuMHB4O3N0cm9rZS1saW5lY2FwOmJ1dHQ7c3Ryb2tlLWxpbmVqb2luOm1pdGVyO3N0cm9rZS1vcGFjaXR5OjEnIC8+CjxwYXRoIGNsYXNzPSdib25kLTIgYXRvbS0yIGF0b20tMycgZD0nTSAxMTguNCwyMDMuMiBMIDkwLjYsMjI4LjcnIHN0eWxlPSdmaWxsOm5vbmU7ZmlsbC1ydWxlOmV2ZW5vZGQ7c3Ryb2tlOiMzQjQxNDM7c3Ryb2tlLXdpZHRoOjIuMHB4O3N0cm9rZS1saW5lY2FwOmJ1dHQ7c3Ryb2tlLWxpbmVqb2luOm1pdGVyO3N0cm9rZS1vcGFjaXR5OjEnIC8+CjxwYXRoIGNsYXNzPSdib25kLTQgYXRvbS0yIGF0b20tNScgZD0nTSAxNDMuOCwxNDYuNiBMIDEzMi4zLDk1LjMnIHN0eWxlPSdmaWxsOm5vbmU7ZmlsbC1ydWxlOmV2ZW5vZGQ7c3Ryb2tlOiMzQjQxNDM7c3Ryb2tlLXdpZHRoOjIuMHB4O3N0cm9rZS1saW5lY2FwOmJ1dHQ7c3Ryb2tlLWxpbmVqb2luOm1pdGVyO3N0cm9rZS1vcGFjaXR5OjEnIC8+CjxwYXRoIGNsYXNzPSdib25kLTMgYXRvbS0zIGF0b20tNCcgZD0nTSA5MC42LDIyOC43IEwgMTMuNiwyMDQuNycgc3R5bGU9J2ZpbGw6bm9uZTtmaWxsLXJ1bGU6ZXZlbm9kZDtzdHJva2U6IzNCNDE0MztzdHJva2Utd2lkdGg6Mi4wcHg7c3Ryb2tlLWxpbmVjYXA6YnV0dDtzdHJva2UtbGluZWpvaW46bWl0ZXI7c3Ryb2tlLW9wYWNpdHk6MScgLz4KPHBhdGggY2xhc3M9J2JvbmQtNSBhdG9tLTUgYXRvbS02JyBkPSdNIDEzMi4zLDk1LjMgTCA1NS4zLDcxLjMnIHN0eWxlPSdmaWxsOm5vbmU7ZmlsbC1ydWxlOmV2ZW5vZGQ7c3Ryb2tlOiMzQjQxNDM7c3Ryb2tlLXdpZHRoOjIuMHB4O3N0cm9rZS1saW5lY2FwOmJ1dHQ7c3Ryb2tlLWxpbmVqb2luOm1pdGVyO3N0cm9rZS1vcGFjaXR5OjEnIC8+Cjx0ZXh0IHg9JzEyMi4zJyB5PScxOTAuMicgY2xhc3M9J2F0b20tMicgc3R5bGU9J2ZvbnQtc2l6ZTozMnB4O2ZvbnQtc3R5bGU6bm9ybWFsO2ZvbnQtd2VpZ2h0Om5vcm1hbDtmaWxsLW9wYWNpdHk6MTtzdHJva2U6bm9uZTtmb250LWZhbWlseTpzYW5zLXNlcmlmO3RleHQtYW5jaG9yOnN0YXJ0O2ZpbGw6IzNCNDE0MycgPkc8L3RleHQ+Cjx0ZXh0IHg9JzE0NC41JyB5PScxOTAuMicgY2xhc3M9J2F0b20tMicgc3R5bGU9J2ZvbnQtc2l6ZTozMnB4O2ZvbnQtc3R5bGU6bm9ybWFsO2ZvbnQtd2VpZ2h0Om5vcm1hbDtmaWxsLW9wYWNpdHk6MTtzdHJva2U6bm9uZTtmb250LWZhbWlseTpzYW5zLXNlcmlmO3RleHQtYW5jaG9yOnN0YXJ0O2ZpbGw6IzNCNDE0MycgPmU8L3RleHQ+CjxwYXRoIGQ9J00gMTUxLjYsMTkyLjYgTCAxNTEuNiwxOTIuNSBMIDE1MS42LDE5Mi40IEwgMTUxLjYsMTkyLjIgTCAxNTEuNSwxOTIuMSBMIDE1MS41LDE5Mi4wIEwgMTUxLjQsMTkxLjggTCAxNTEuMywxOTEuNyBMIDE1MS4yLDE5MS42IEwgMTUxLjIsMTkxLjUgTCAxNTEuMSwxOTEuNCBMIDE1MC45LDE5MS4zIEwgMTUwLjgsMTkxLjIgTCAxNTAuNywxOTEuMiBMIDE1MC42LDE5MS4xIEwgMTUwLjQsMTkxLjEgTCAxNTAuMywxOTEuMCBMIDE1MC4yLDE5MS4wIEwgMTUwLjAsMTkxLjAgTCAxNDkuOSwxOTEuMCBMIDE0OS44LDE5MS4wIEwgMTQ5LjYsMTkxLjEgTCAxNDkuNSwxOTEuMSBMIDE0OS40LDE5MS4xIEwgMTQ5LjIsMTkxLjIgTCAxNDkuMSwxOTEuMyBMIDE0OS4wLDE5MS40IEwgMTQ4LjksMTkxLjUgTCAxNDguOCwxOTEuNiBMIDE0OC43LDE5MS43IEwgMTQ4LjYsMTkxLjggTCAxNDguNiwxOTEuOSBMIDE0OC41LDE5Mi4wIEwgMTQ4LjUsMTkyLjIgTCAxNDguNCwxOTIuMyBMIDE0OC40LDE5Mi40IEwgMTQ4LjQsMTkyLjYgTCAxNDguNCwxOTIuNyBMIDE0OC40LDE5Mi44IEwgMTQ4LjQsMTkzLjAgTCAxNDguNSwxOTMuMSBMIDE0OC41LDE5My4yIEwgMTQ4LjYsMTkzLjQgTCAxNDguNiwxOTMuNSBMIDE0OC43LDE5My42IEwgMTQ4LjgsMTkzLjcgTCAxNDguOSwxOTMuOCBMIDE0OS4wLDE5My45IEwgMTQ5LjEsMTk0LjAgTCAxNDkuMiwxOTQuMCBMIDE0OS40LDE5NC4xIEwgMTQ5LjUsMTk0LjIgTCAxNDkuNiwxOTQuMiBMIDE0OS44LDE5NC4yIEwgMTQ5LjksMTk0LjIgTCAxNTAuMCwxOTQuMiBMIDE1MC4yLDE5NC4yIEwgMTUwLjMsMTk0LjIgTCAxNTAuNCwxOTQuMiBMIDE1MC42LDE5NC4xIEwgMTUwLjcsMTk0LjEgTCAxNTAuOCwxOTQuMCBMIDE1MC45LDE5My45IEwgMTUxLjEsMTkzLjkgTCAxNTEuMiwxOTMuOCBMIDE1MS4yLDE5My43IEwgMTUxLjMsMTkzLjUgTCAxNTEuNCwxOTMuNCBMIDE1MS41LDE5My4zIEwgMTUxLjUsMTkzLjIgTCAxNTEuNiwxOTMuMCBMIDE1MS42LDE5Mi45IEwgMTUxLjYsMTkyLjggTCAxNTEuNiwxOTIuNiBMIDE1MC4wLDE5Mi42IFonIHN0eWxlPSdmaWxsOiMwMDAwMDA7ZmlsbC1ydWxlOmV2ZW5vZGQ7ZmlsbC1vcGFjaXR5OjE7c3Ryb2tlOiMwMDAwMDA7c3Ryb2tlLXdpZHRoOjAuMHB4O3N0cm9rZS1saW5lY2FwOmJ1dHQ7c3Ryb2tlLWxpbmVqb2luOm1pdGVyO3N0cm9rZS1vcGFjaXR5OjE7JyAvPgo8L3N2Zz4K data:image/svg+xml;base64,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 CC[Ge](CC)CC 0 title abstract description 10
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic System
- C07F7/02—Silicon compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic System
- C07F9/02—Phosphorus compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F3/00—Compounds containing elements of Groups 2 or 12 of the Periodic System
- C07F3/10—Mercury compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/093—Preparation of halogenated hydrocarbons by replacement by halogens
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F5/00—Compounds containing elements of Groups 3 or 13 of the Periodic System
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B35/00—Boron; Compounds thereof
- C01B35/08—Compounds containing boron and nitrogen, phosphorus, oxygen, sulfur, selenium or tellurium
- C01B35/10—Compounds containing boron and oxygen
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B17/00—Sulfur; Compounds thereof
- C01B17/64—Thiosulfates; Dithionites; Polythionates
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B21/00—Nitrogen; Compounds thereof
- C01B21/082—Compounds containing nitrogen and non-metals and optionally metals
- C01B21/083—Compounds containing nitrogen and non-metals and optionally metals containing one or more halogen atoms
- C01B21/084—Compounds containing nitrogen and non-metals and optionally metals containing one or more halogen atoms containing also one or more oxygen atoms, e.g. nitrosyl halides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/06—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom containing only hydrogen and carbon atoms in addition to the ring nitrogen atom
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Kraus et al. | Aliphatic germanium derivatives. I. Triethylgermanium compounds; some of their properties and reactions | |
Douglass et al. | Superior method for preparing sulfinyl chlorides | |
Kraus et al. | Chemistry of the trimethyltin group | |
Kraus et al. | Studies relating to organic germanium derivatives. IV. diphenyl germanium and octaphenyl germanopropane | |
Aubke et al. | Iodine Fluorosulfates | |
Friedrich et al. | The reaction between alkali metal alkyls and quaternary arsonium compounds | |
Brower et al. | Methylsulfur Trichloride1 | |
Benkeser et al. | The True Identity of the Solvated Free Radical “Triphenylsilicyl Ethylammine.” The Multiple Addition of Lithium to an Aromatic System in Ethylamine | |
Marvel et al. | The Preparation of Dialkyl Mercury Compounds from the Grignard Reagent. II. The Relative Stability of the Carbon-Mercury Linkage in Dialkyl Mercury Compounds | |
Maynard | The Action of Mercury on Organic Iodides. I. The Formation of Methylmercuric Iodide and Benzylmercuric IODIDE1 | |
Anderson | XIV.—On the constitution and properties of picoline, a new organic base from coal-tar | |
Jones et al. | 10. Some physical properties of the alkyl compounds of mercury, tin, and lead | |
Morgan et al. | CXV.—Researches on residual affinity and co-ordination. Part V. Gallium acetylacetone and its analogues | |
Ives et al. | 203. The preparation, properties, and chlorination products of carbon diselenide | |
Kraus et al. | Studies Relating to Organic Germanium Derivatives. III. Diphenyl Germanium Dihalides and Diphenyl Germanium Imine | |
Milligan et al. | Chemistry of the Tris-(triphenylgermanyl)-silyl Group1 | |
Flood | Aliphatic Germanium Derivatives. II. Diethyldiphenylgermane, Diethylgermanium Oxide and Diethylgermanium Dibromide | |
US2739165A (en) | Stabilization of aromatic chlorosilanes | |
Kinney et al. | Organoboron—Nitrogen Compounds. II. The Reaction of Boron Chloride with p-Toluidine | |
Dennis et al. | Germanium. XXXIV. Trimethyl Germanium BROMIDE1 | |
McGrath et al. | The Reaction of Boron Fluoride with Water. I. Preparation and Some Properties of Pure Boron Fluoride Dihydrate1 | |
Hager et al. | The valence of nitrogen in quaternary ammonium compounds | |
Aynsley et al. | The preparation and properties of tellurium dibromide | |
Anderson | Bis-(triethylgermanium) Sulfate and Diethylgermanium Sulfate | |
Lenher et al. | The Preparation of Selenium Monochloride and Monobromide |