Lithium copper oxide, primary

The impedance of small lithium-copper oxide primary cells has been investigated in a frequency range from 5 mHz to 10 kHz. The cells had been stored after assembly for from three weeks up to three years and their state of charge was from 100% down to 20%. After an initial period of electrochemical stabilization, the cells exhibited consistent results and the shape of the impedance locus was found to depend markedly on the state of charge of the cell. An interpretation of the results is given in terms of an analogue circuit which contains components to represent the contribution to the impedance of each electrode and of the electrolyte. 

Lithium-copper oxide primary cells have been established since 1969 as a versatile and reliable power source in a range of applications. 

Primary lithium-thionyl chloride M. lost (also lithium-iron disulphide, lithium-copper oxide, lithium-sulphur dioxide, lithium-vanadium pentoxide, lithium-manganese dioxide, lithium-lead bismuthate, lithium-silver chromate)... 

These researches opened the door to the fabrication and commercialization of varieties of primary hthium batteries since the late l%0s nonaqueous hthium cells, especially the 3-V primary systems, have been developed. These systems include lithium-sulfur dioxide (Li//S02) cehs, lithium-polycarbon monofluoride (Li//(CF t) ) cells introduced by Matsuschita in 1973, lithium-manganese oxide (Li//Mn02) cells commercialized by Sanyo in 1975, lithium-copper oxide (Li//CuO) cells, lithium-iodine (Li//(P2VP)1J cells. During the same period, molten salt systems (LiCl-KCl eutecticum) using a Li-Al alloy anode and a FeS cathode were introduced [1]. The lithium-iodine battery has been used to power more than four million cardiac pacemakers since its introduction in 1972. During this time the lithium-iodine system has established a record of reliability and performance unsurpassed by any other electrochemical power source [18]. 

Lithium dialkylcopper reagents can be oxidized to symmetrical dimers by O2 at -78°C in THF. The reaction is successful for R = primary and secondary alkyl, vinylic, or aryl. Other oxidizing agents (e.g., nitrobenzene) can be used instead of O2. Vinylic copper reagents dimerize on treatment with oxygen, or simply on standing at 0°C for several days or at 25°C for several hours, to yield LS-dienes." ... 

Alkyl halides (particularly bromides) undergo oxidative addition with activated copper powder, prepared from Cu(I) salts with lithium naphthalenide, to give alkylcopper species10. The alkyl halides may be functionalized with ester, nitrile and chloro functions ketone and epoxide functions may also be tolerated in some cases11. The resulting alkylcopper species have been shown to react efficiently with acid chlorides, enones (conjugate addition) and (less efficiently) with primary alkyl iodides and allylic and benzylic bromides (equations 5 and 6). If a suitable ring size can be made, intramolecular reactions with epoxides and ketones are realized. 

The stannylcupration of alkynes has been widely studied. Reaction of alkynes with lithium bis(tributylstannyl) cuprate leads to r -2-(tri butyl stannyl) vinyl cuprates, which are synthetically equivalent to cis- 1,2-ethylene dianions. Addition of the tin-copper reagent across the triple bond occurs i>7/-stereospecifically, thus providing Z-vinylstannanes. Phenylacetylene reacts with the tin cuprate with a regiochemistry opposite to that of 1-decyne.294 The intermediate cuprates react well with the various electrophiles.295 For example, the reaction with ethylene oxide gives primary alcohols, and further treatment of their />-toluenesulfonates with butyllithium gives 1-substituted cyclobutenes (Equation (120)) 294... 

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