ライフサイエンスコーパス: alkali metal

1 decrease of the ionization potential of the alkali metal.

2 apacity for Na but a high capacity for other alkali metals.

3 the chains depend on the structure-directing alkali metals.

4 ctra of analogous ions containing monovalent alkali metals.

5 only observed in electrochemical doping with alkali metals.

6 y in miniaturization, and interferences from alkali metals.

7 ]cumulene ([3]TrTol) has been explored using alkali metals.

8 ntered cubic lattice, which is common to all alkali metals.

9 pproach has been realized using a rare earth/alkali metal/1,1'-BINOLate (REMB) heterobimetallic frame

10 kaline-earth metal), AFe(2)As(2), AFeAs (A = alkali metals), A(3)M(2)O(5)Fe(2)As(2) (M = transition m

11 d clusters (MPCs), Au25(SC2Ph)18, containing alkali metal acetate salts (MOAc) produce spectra in whi

12 methyl ketones, malononitrile, bromine, and alkali metal acetates is reported.

13 stic charge-remote fragmentation patterns of alkali metal-adducted fatty acids following high energy

14 r [M + K](+) ions of the FFAs, whereas other alkali metal adducts can be generated by treating the wi

15 Primarily protonated molecular ions and alkali metal adducts were observed in the mass spectra.

16 ions reduce to Cu(I), Ni(I), and Fe(I) upon alkali metal adsorption, whereas Mn maintains its formal

17 Direct electron transfer would imply that alkali metal alkoxides are willing partners in these ele

18 oarenes with arenes, triggered by the use of alkali metal alkoxides in the presence of an organic add

19 hodes but also broadens the understanding of alkali metal alloys and hybrid-ion battery chemistry.

20 s pulled out to a greater extent than in the alkali metals alone.

21 Examples of hetero-alkali-metal amides, an increasingly important compositi

22 letely different structural motif within the alkali metal amidotrihydroborate group.

23 Alkali metals, amines and alkanolamines are separated on

24 llowing in situ the reactions of solids with alkali metal/ammonia solutions, using time-resolved X-ra

25 lline K(4)GeP(4)Se(12) outperforms the other alkali metal analogues and exhibits the strongest second

26 own to function as a paracellular barrier to alkali metal and divalent cations.

27 nly stable binary compound formed between an alkali metal and nitrogen, lithium nitride possesses rem

28 (Z)-diazeniumdiolation products, namely, the alkali metal and NMe(4)(+) salts of methyl and ethylbute

29 The ions studied include the alkali metal and tetraalkylammonium cations, halide and

30 Beyond simple alkali metals and ammonium, chemically diverse cations i

31 ded a range of ammonium or imidazolium ions, alkali metals and coordination compounds.

32 hich may be present in solutions composed of alkali metals and ethylenediamine.

33 abundance in the host rocks, such as carbon, alkali metals and halogens, illustrates a feedback betwe

34 that have been prepared using the different alkali metals and may indicate differences in the relati

35 Alkali metals and their alloys can be protected from spo

36 nherent high selectivity for lead over other alkali-metal and alkaline-earth-metal ions.

37 steric effects, oxidation level, presence of alkali metals, and coordination number of the iron atoms

38 be thought of as an ion pair formed from an alkali metal anion (M(-)) and solvated cation (M(en)(3)(

39 Electrochemical cells based on alkali metal anodes are receiving intensive scientific i

40 Alkali metals are beneficial at low concentrations, wher

41 Light alkali metals are generally most easily intercalated due

42 Alkali metals are inherent constituents of biofuels.

43 nitrogen with trivalent lanthanide salts and alkali metals are strong reductants in their own right a

44 The alkali fullerides, A(3)C(60) (A = alkali metal) are molecular superconductors that undergo

45 Sodium can be used as the alkali metal as well as potassium.

46 nces in the results obtained using different alkali metals as reductants (Na, K, Rb, Cs).

47 Here we show that these alkali metals-as single crystals-can grow out of and ret

48 o tune the properties of 2DESs by depositing alkali metal atoms.

49 lectron doping through in situ deposition of alkali-metal atoms, angle-resolved photoemission spectra

50 re metathetical reactions between N5SbF6 and alkali metal azides in different solvents, resulting in

51 isphosphite ligands combined with a suitable alkali metal BArF salt as a regulation agent (RA) provid

52 Shibasaki's rare earth alkali metal BINOLate (REMB) catalysts (REMB; RE = Sc, Y

53 Molten alkali metal borates embody a new class of high-temperat

54 Addition of alkali metal borates to 1 afforded the alkali metal disi

55 s and binding profiles indicate formation of alkali metal-bridged dimers.

56 bimetallic formulations that also contain an alkali metal but in company with another metal.

57 alloys as an anode, the dendritic growth of alkali metals can be eliminated thanks to the deformable

58 A series of alkali metal capped cerium(IV) imido complexes, [M(solv)

59 s of amides involving the direct coupling of alkali metal carboxylate salts with amines is described.

60 oles of the adsorbed hydroxyl (OH(ad))-water-alkali metal cation (AM(+)) adducts, on the basis of the

61 NAPA-MS also favored more extensive alkali metal cation adduction relative to MALDI-MS, with

62 proach is used, where the synergy between an alkali metal cation and a polar solvent leads to high-qu

63 The alkali metal cation and various negative ions are observ

64 ed, enabled by tunable hemilability based on alkali metal cation binding with a macrocyclic "pincer-c

65 nd, the results suggest that the size of the alkali metal cation can control the number of Fe atoms t

66 se observed with recently published diboryne/alkali metal cation complexes.

67 abeling) point to a bridging function for an alkali metal cation connecting the sulfonate anion and a

68 f "alkali control," where the presence of an alkali metal cation enables the reduction of N2 under mi

69 nown to be influenced by the identity of the alkali metal cation in the electrolyte; however, a satis

70 M.2 concentration and a strong effect of the alkali metal cation M(+).

71 Alkali metal cation selectivity of the proton-activated

72 r mild conditions, and then chelation of the alkali metal cation uncovers a highly reactive species t

73 r the An[Co(OH2)(6-6m)][Fe(CN)6]m.xH2O (An = alkali metal cation) family of three-dimensional Prussia

74 d by the diastereomers when cationized by an alkali metal cation, [M + X](+) where X = Li, Na, K, and

75 Even capped with an alkali metal cation, poor orbital energy matching and ov

76 ond was observed with increasing size of the alkali metal cation.

77 etallic pocket, closely interacting with the alkali metal cation.

78 e charge from partial (NO(2)) bonding to the alkali-metal cation.

79 The gas-phase structures of protonated and alkali metal cationized arginine (Arg) and arginine meth

80 raction with the N terminus as zwitterionic, alkali metal cationized arginine, yet both are unambiguo

81 ermore, the unique structures adopted by the alkali metal-cationized cis- and trans-proline variants

82 it was observed that the resolution between alkali metal-cationized cis- and trans-proline variants

83 ons than for ArgGly is due to the ability of alkali metal-cationized GlyArg to adopt a nearly linear

84 determining the structures of protonated and alkali metal-cationized glycyl-L-arginine (GlyArg) and L

85 The effect of alkali metal cations (Li(+) , Na(+) , K(+) , Cs(+) ) on

86 can be rationalized as Zintl phases with 14 alkali metal cations A(+) (A = K, Rb), two tetrahedral [

87 oxide) spacer lengths between phthalates and alkali metal cations as counterions are designed for imp

88 The role of the alkali metal cations in halide perovskite solar cells is

89 mical calculations that encapsulation of the alkali metal cations in the cavity of 1 predominantly oc

90 ions in the absence or presence of different alkali metal cations in the matrix, discrete lipid class

91 was orders of magnitude below the number of alkali metal cations in the zeolites but was similar to

92 functional theory calculations show that the alkali metal cations influence the distribution of produ

93 e molecule is found to encapsulate the light alkali metal cations Li(+) and Na(+) in the absence of a

94 g an organic cation and crown-ether chelated alkali metal cations show that specific adsorption of me

95 are subsequently stabilized by intercalated alkali metal cations that reside in the one-dimensional

96 nteractions and of cation/pi interactions of alkali metal cations with aromatic rings was conducted.

97 hly sensitive to increased concentrations of alkali metal cations, a situation that remains unexplain

98 Addition of neutral boranes, alkali metal cations, and an Fe(2+) complex increases th

99 twork of gamma-cyclodextrins (gamma-CDs) and alkali metal cations, can separate a wide range of benze

100 w that direct lipid bilayer translocation of alkali metal cations, Cl(-), and a charged arginine side

101 opensities of inorganic cations, such as the alkali metal cations, have received relatively little at

102 take, storage, and efflux mechanisms for the alkali metal cations, Na(+) and K(+), the divalent catio

103 with what was known from the complexation of alkali metal cations.

104 1 in 2 days, without the need for additional alkali metal cations.

105 amma-CD)(6) cubes linked by eight-coordinate alkali metal cations.

106 bute to the sensitivity of exomer mutants to alkali metal cations.

107 metal cations (e.g., Co(2+) and Ni(2+)) over alkali-metal cations (Li(+) and Na(+)).

108 novel ternary Zintl phase Li3NaGe2 comprises alkali-metal cations and [Ge2](4-) dumbbells.

109 rements to investigate adsorption of several alkali-metal cations at the interface with graphene and

110 7.24-nm(3) cavities containing exchangeable alkali-metal cations that can be replaced by transition-

111 h membranes decay rapidly in the presence of alkali-metal cations, but can be maintained in the absen

112 nic frameworks (CD-MOFs) in a combination of alkali-metal cations.

113 These I-V-VI(2) ternary alkali-metal chalcoarsenates have infinite single chains

114 of these results, we propose a mechanism for alkali metal charge reduction of membrane proteins.

115 This suggests the importance of the alkali metal chelating agent in the reversibility of din

116 cal reaction in secondary batteries based on alkali metal chemistries.

117 olecular organometallic compounds with mixed-alkali-metal cluster cores, LiK5 and Li3 K3 , sandwiched

118 Experiments with crown ether-alkali metal complexes confirm the validity of the model

119 The alkali-metal complexes prefer open-cage structures with

120 Since alkali-metal compounds are often not the end products of

121 ions indicate that reduction of the iron and alkali metal coordination cooperatively weaken the N-N b

122 Herein, we explore the impact of alkali metal counter cations on hydroxide solvation and

123 f the molecular salts are independent of the alkali metal counterions and have a value of 2.0 eV for

124 ido complexes demonstrated the impact of the alkali metal counterions on the geometry of the [Ce hori

125 on are known to be stable in the presence of alkali metal counterions.

126 on of alkali metal borates to 1 afforded the alkali metal disilicon(0) borates 1M[BAr4] (M = Li, Ar =

127 Birch reductions traditionally employ alkali metals dissolved in ammonia to produce a solvated

128 ginating from steadily increasing amounts of alkali metals dissolved in refrigerated liquid ammonia m

129 Alkali metal dopants greatly improve perovskite performa

130 a systematic investigation of the effects of alkali metal doping on the charge state and crystal fiel

131 ivity of N(2) with Li, compared to the other alkali metals, e.g., Na and K.

132 Whereas alkali metal enolates fail, owing to facile deacylation,

133 nd with zinc enolates generated by quenching alkali metal enolates of esters with zinc chloride.

134 This use of zinc enolates, instead of alkali metal enolates, greatly expands the scope of amid

135 The use of zinc enolates, instead of alkali metal enolates, greatly expands the scope of the

136 very selective (approximately 80%) over the alkali-metal exchanged materials.

137 in which a neutral molecule binds the light alkali metals exclusively through cation-pi interactions

138 presence of montmorillonite and other salts, alkali metal fluorides did not yield any detectable olig

139 bly to traditional halex fluorinations using alkali metal fluorides, which generally require temperat

140 ase-transfer catalysts for fluorination with alkali metal fluorides.

141 ydride complexes, providing a high-yielding, alkali metal-free route to strongly activated early-meta

142 e the well-studied face-centered cubic A3C60 alkali metal fulleride superconductors.

143 Superconductivity in the A(3)C(60) (A = alkali metal) fullerides has been exclusively associated

144 on of the corresponding arylmetal halides by alkali metal/graphite (Zn or Hg) or sodium hydride (Cd).

145 Herein we demonstrate that the presence of alkali metal halide salts, in conjunction with low coppe

146 rowth promoters (e.g., organic molecules and alkali metal halides) to facilitate the layered growth o

147 ganic diradicals, and the way to think about alkali metal halides, show us the way to integrate simul

148 wever, the galvanic replacement chemistry of alkali metals has rarely been explored.

149 olymeric anionic chains, but the size of the alkali-metals has a profound effect on the packing of th

150 r a third oxidation state, -1, of all of the alkali metals heavier than lithium.

151 active CF3(-) adduct can be synthesized from alkali metal hydride, HCF3, and borazine Lewis acids in

152 Light alkali metal hydridotriphenylborates M[HBPh3] (M = Li, N

153 5a-o, and 6a-e using superbasic solutions of alkali-metal hydroxides in DMSO is described.

154 , lithium has always been the most important alkali metal in organometallic chemistry.

155 The optical absorption spectra of alkali metals in ethylenediamine have provided evidence

156 Alkali metals in silica gel (the Na(2)K-SG(I) reagent) c

157 also used to study the other A(2)PtH(6) (A = alkali metal) including, the at present, unknown Li salt

158 scovered phenomena such as complex phases of alkali metals, incommensurate host-guest structures, and

159 of face-centred-cubic (f.c.c.) A(3)C(60) (A=alkali metal) increases monotonically with inter C(60) s

160 Three alkali-metal-indium compounds K34In(92.30)Li(12.70) (I),

161 ectrocatalyst was assembled with a different alkali metal intercalated between two nanosheets (NS) of

162 there is significant interest in addressing alkali-metal-intercalated aromatic hydrocarbons, in whic

163 s the electronic and optical transitions, in alkali-metal-intercalated molecular electronic crystals.

164 The synthetic and crystal chemistry of alkali metal intercalation into PAHs differs from that i

165 Alkali metal intercalation into polyaromatic hydrocarbon

166 pramolecular aggregate with a high degree of alkali metal intercalation.

167 ny atomic analogue, is isomorphic to certain alkali-metal intercalation compounds of fullerene C(60)

168 debundling results from intercalation of the alkali metal into the SWNT ropes.

169 ns (Ln=rare earth metal; A=anionic ligand; M=alkali metal) involving reduction of Sc(NR2 )3 with K in

170 lectively determined KI compare to different alkali metal iodides: NaI, RbI, CsI; also investigation

171 itional noncovalent interactions between the alkali metal ion and the nucleobases.

172 e in the proton affinity, an increase in the alkali metal ion binding affinities, an increase in the

173 In addition, alkali metal ion binding is expected to lead to an incre

174 The analytes are observed as the alkali metal ion complexes.

175 The alkali metal ion selectivities of the 12 hexamers were e

176 crown-6 ether)(H(2)O)(1-4) complexes for the alkali metal ion series were probed using infrared predi

177 ation of a supramolecular system "Pt complex-alkali metal ion"; the latter is supported by restoratio

178 Bond dissociation energies of alkali metal ion-halouracil complexes, M+(XU), are deter

179 the three-dimensional structure of hydrated alkali-metal ion clusters.

180 an serve as ideal anodes for 'Rocking-Chair' alkali metal-ion batteries.

181 ntly used as negative electrode material for alkali-metal-ion batteries, similar to its oxide analogu

182 4) that form discrete molecular species with alkali metal ions (M(+) = Li(+), Na(+), K(+)).

183 usters, was used to record depth profiles of alkali metal ions (Me(+)) within thin SiO2 layers.

184 monium ions (weak ion pairing) contrast with alkali metal ions (strong ion pairing).

185 The effect of other alkali metal ions (such as Li and K) on the enantioselec

186 In conventional intercalation cathodes, alkali metal ions can move in and out of a layered mater

187 5) and CsBi(3)Se(5) have stepped layers with alkali metal ions found disordered in several trigonal p

188 ity of the title compounds to associate with alkali metal ions in solution and the gas phase has demo

189 uracil and its noncovalent interactions with alkali metal ions is investigated both experimentally an

190 M(+) include the alkali metal ions Na(+) and K(+).

191 d that differences in folding with different alkali metal ions observed at high concentration arise f

192 Binding of alkali metal ions to the 3,4-ethylenedioxythiophene (EDO

193 the positive mode involves the depletion of alkali metal ions via ion evaporation of metal ions solv

194 For identically charged alkali metal ions, electrostatic charge densities based

195 ion was achieved after adduct formation with alkali metal ions, however, and efficiency was shown to

196 as a "bridge" between the smaller and larger alkali metal ions, is consistent with the well-known spe

197 reover, FeSe-based systems intercalated with alkali metal ions, NH3 molecules or organic molecules ar

198 ing models, no size dependence for the other alkali metal ions.

199 p system will accumulate SO4(2-), Cl(-), and alkali metal ions.

200 nt proline isomeric molecules complexed with alkali metal ions.

201 d G4DNA in the presence of 100 mM monovalent alkali metal ions.

202 ee hosts and their host.guest complexes with alkali metal ions.

203 s as a bridge between the larger and smaller alkali metal ions.

204 mmable polymer nitrocellulose patterned with alkali metal ions; this pattern encodes the information.

205 e alkaline-earth ions Ba(2+) and Ca(2+), the alkali-metal ions Li(+), Na(+), K(+), and Cs(+), and the

206 Extraction efficiencies for alkali-metal ions were lower than those for dibenzo-18-c

207 e organocations, as opposed to, for example, alkali-metal ions, play a pivotal role in reorganizing t

208 ntral five-membered ring, for binding of six alkali-metal ions.

209 terms of synergistic effects, for which the alkali metal is essential, though it is often the second

210 otassium (Na-K) liquid alloy composed of two alkali metals is one of the ideal alternatives for Li me

211 three groups, independent of the associated alkali metal (K or Na).

212 benzo-fused double [7]helicene (1) with two alkali metals, K and Rb, provided access to three differ

213 Altogether, tuning the Li state in the alkali metal layer presents a promising way for modifica

214 ansition metal layer and a deficiency in the alkali metal layer.

215 ology offers a solution toward the design of alkali metal layered oxides.

216 splacement of transition metal ions into the alkali metal layers has been proposed to explain the fir

217 In this process, earth abundant, alkali metal Lewis base catalyst plays a dual role.

218 utral HAT process involving hydrosilanes and alkali metal Lewis base catalysts - eliminating the use

219 th" that has been applied to measure BDEs of alkali metal (Li+) adducts and halide (Cl-) adducts of m

220 lated InsPs have a much greater affinity for alkali metals (Li(+) > Na(+) > K(+)) than quaternary amm

221 ere we describe its intercalation by several alkali metals (Li, K, Rb and Cs) and alkali-earth Ca.

222 Instead of using heavy alkali metals, Li is herein shown to give the highest ra

223 Different alkali metals like Na, Li and Rb were incorporated in CZ

224 tron reduction of [Co(II)((R)salophen)] with alkali metals (M = Li, Na, K) leads to either ligand-cen

225 mination of the known SHG active AMCO3F (A = alkali metal, M = alkaline earth metal, Zn, Cd, or Pb) m

226 Addition of low concentrations of alkali metals may provide an advantageous approach for c

227 s with extended pai-conjugation, prepared by alkali metal-mediated reduction of several aromatic and

228 A straightforward alkali-metal-mediated hydroamination of styrenes using b

229 Combining alkali-metal-mediated metalation (AMMM) and N-heterocycl

230 Here, this "alkali-metal-mediated" chemistry is surveyed focusing ma

231 y challenged by sodium and potassium, as the alkali-metal mediation of organic reactions in general h

232 unity to this rising unifying phenomenon of "alkali-metal mediation".

233 c in that magnesiation can only work through alkali-metal mediation, these reactions add magnesium to

234 ve strong mass spectra of molecular ions and alkali metal molecular ion adducts, with lower Na and K

235 s common to prior research in the field with alkali metal nitrate molten salt electrolytes and operat

236 A facile synthesis of heavy alkali metal octahydrotriborates (MB(3) H(8) ; M=K, Rb,

237 The controlled reaction of Na and Cs, two alkali metals of different ionic sizes and binding abili

238 ASIC1a shows a selectivity sequence for alkali metals of Na(+)>Li(+)>K(+)>>Rb(+)>Cs(+).

239 Anions play a crucial role in locking alkali metals on the interior of metal-organic capsules

240 ish that reduction of ((i)PrPDI)FeCl(2) with alkali metal or borohydride reagents results in sequenti

241 ly on bimetallic formulations containing two alkali metals or an alkali metal paired with magnesium,

242 We have synthesized a series of new alkali-metal or Tl(+) titanium iodates, A(2)Ti(IO(3))(6)

243 cations, however, aggregates composed of the alkali metal-oxide cations template various cage compoun

244 Alkali metal-oxygen batteries are of great interests for

245 mulations containing two alkali metals or an alkali metal paired with magnesium, calcium, zinc, alumi

246 Like other alkali-metal pyroxenes with S > (1)/(2), NaMnGe(2)O(6) (

247 nds with the general formula ABi(3)Q(5) (A = alkali metal; Q = chalcogen).

248 rn Tibet (China) are highly enriched in rare alkali metals (RAM).

249 s demonstrates that the Ln[N(SiMe(3))(2)](3)/alkali metal reaction can mimic divalent lanthanide redu

250 al chemical reactions that typically require alkali metal reductants and can be used in other organic

251 The implications of the LnZ(3)/alkali metal reduction chemistry on the mechanism of din

252 The solution phase alkali metal reduction of [8]annulenyl isocyanate (C8H7N

253 ed by either alkane reductive elimination or alkali metal reduction of a suitable zirconium(IV) dihal

254 This LnZ(3)/alkali metal reduction system provides crystallographica

255 road oscillations in the PDF show that added alkali metals remain in the pores as nanoscale metal clu

256 C) can be further improved threefold through alkali metal salt promotion treatment.

257 ne polymer electrolytes containing different alkali metal salts (Na(+), K(+) and Rb(+)), including th

258 The alkali metal salts are not amenable for recrystallizatio

259 embrane proteins, we examined the utility of alkali metal salts as a charge-reducing agent.

260 Low concentrations of alkali metal salts caused marked charge reduction in the

261 The required alkali metal salts M(2)[DBA] are readily accessible from

262 was evaluated using several inorganic salts (alkali metal salts of chloride) and a weak acid of commo

263 of p-tert-butylcalix[4]arene (Bu(t)C4), the alkali metal salts of monoanionic Bu(t)C4 exist in monom

264 rough metathesis reaction between halide and alkali metal salts of two cationic and three anionic Ir

265 Addition of alkali metal salts to this zirconium hydrosilazide compo

266 The affinity of these hosts for alkali metal salts were evaluated in solution (CD(3)CN),

267 omposed of gamma-cyclodextrin (gamma-CD) and alkali metal salts--namely, CD-MOF.

268 The alkali-metal salts (potassium and sodium) of a large num

269 lated for the first time as pure crystalline alkali-metal salts.

270 vided a method to obtain rates of ligand and alkali metal self-exchange in the RE/Li frameworks, demo

271 rease in DNA electrophoretic mobility in the alkali metal series, Li(+) < Na(+) < K(+) < Rb(+).

272 bles: (1) identification of stable, isolable alkali metal silanolates, (2) identification of conditio

273 It was found that the alkali metal silanolates, either isolated or formed in s

274 containing anions are common in concentrated alkali-metal silicate solutions, but reveal no evidence

275 ther with evidence for a mechanism involving alkali metal silylenoid intermediates.

276 the organic derivatives of the other common alkali metals sodium and potassium have proved indispens

277 tionalization catalysed by an Earth-abundant alkali metal species.

278 When defects are present, alkali metals strongly bind to them.

279 can cause large electron transfer from light alkali metals such as Li to Cs, causing Cs to become ani

280 roscopic analysis of the separate effects of alkali metal sulfates (Na2SO4, Rb2SO4), GdmCl, and Gdm2S

281 aceted role in a variety of media, including alkali metal-sulfur batteries, aqueous solutions at high

282 derable attentions for their applications in alkali metals-sulfur batteries.

283 alkali-metal-sulfur batteries, organic syntheses, biolog

284 -generated models reveal that on addition of alkali metal the solvent molecules form voids of approxi

285 CO on Au in an MHCO(3) buffer (where M is an alkali metal), the experimentally measured local basicit

286 specific capacity and low redox potential of alkali metals, their practical application as anodes is

287 eristics here are close to those in numerous alkali-metal-Tl cluster systems.

288 Our system uses the thermal excitation of alkali metals to transmit an encoded signal over long di

289 hemical reactions--the thermal excitation of alkali metals--to transmit coded alphanumeric informatio

290 involving reduction of trivalent salts with alkali metals used with lanthanides can also be applied

291 ped magnetometers (OPMs) based on lasers and alkali-metal vapor cells are currently the most sensitiv

292 Alkali metal vapors enable access to single electron sys

293 anium(II) or terphenyltin(II) chlorides with alkali metals was investigated.

294 The reaction mechanisms for the heavy alkali metals were investigated both experimentally and

295 tion metalate of the series A(x)MnO(2), (A = alkali metal) where a complete 1:1 charge ordering of Mn

296 clear nitride, complete encapsulation of the alkali metal with cryptand provides the terminally bound

297 ity in materials obtained by the reaction of alkali metals with polyaromatic hydrocarbons, such as ph

298 rearrangement of electronegativities of the alkali metals with pressure, with Na becoming the most e

299 It is simply based on reactions of the pure alkali metals with THF.BH(3) , does not require the use

300 benefit of reducing common adducts, such as alkali metals, without the addition of solution additive