ライフサイエンスコーパス: alkali metal

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

2 ctra of analogous ions containing monovalent alkali metals.

3 only observed in electrochemical doping with alkali metals.

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

5 ether it can be replaced by any of the other alkali metals.

6 contain variable amounts of easily ionizable alkali metals.

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

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

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

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

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

12 face-adsorbed tributyl phosphate (TBP) as an alkali metal adduct has been investigated.

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

14 s spectrometry is hindered by two processes: alkali metal adduction and fragmentation of the intact i

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

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

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

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

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

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

21 Alkali metal amides typically aggregate in solution and

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

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

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 hows minimal interference effects from other alkali metal and alkaline earth metal cations and has go

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

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 rt, we show that direct interactions between alkali metals and arenes occur at or within the van der

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 Light alkali metals are generally most easily intercalated due

40 Alkali metals are inherent constituents of biofuels.

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

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

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

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

45 Different alkali metal atoms are observed to donate electrons to C

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

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

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

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

50 of substituted calixarenes was screened for alkali-metal-binding selectivity.

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

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

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

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

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

56 The alkali metal cation and various negative ions are observ

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

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

59 Binding constants of several crown ether-alkali metal cation complexes that were previously studi

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

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

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

63 3-methylimidazolium hexafluorophosphate, the alkali metal cation extraction selectivity and efficienc

64 With X = trifluoromethyl, effective alkali metal cation extractions from acidic, neutral, an

65 and 18-crown-6 are utilized for competitive alkali metal cation extractions from aqueous solutions i

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

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

68 Alkali metal cation selectivity of the proton-activated

69 at include M-M-C angle, Coulombic repulsion, alkali metal cation size, and the character of the molec

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

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

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

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

74 Finally, the biological implications of the alkali metal cation-pi interaction are addressed.

75 The alkali metal cation-pi interaction is a force of potenti

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

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

78 plexed through their hydroxyl groups to each alkali metal cation.

79 ch serves as the primary binding site for an alkali metal cation.

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

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

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

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

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

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

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

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

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

89 hides and selenides containing highly mobile alkali metal cations as charge-balancing extra-framework

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

91 ds, NH(3) and pyrimidine, and to results for alkali metal cations bound to adenine.

92 ere obtained as contact ion triples with two alkali metal cations complexed between aryl rings.

93 Only the larger alkali metal cations form tight ion pairs with the trian

94 remarkable color response upon extraction of alkali metal cations from basic aqueous solutions into c

95 analysis of the complexes of 18-crown-6 with alkali metal cations in an ESI quadrupole ion trap mass

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

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

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

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

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

101 Recent work has suggested that alkali metal cations may be coordinated by pi systems, s

102 The alkali metal cations Na(+) and K(+) have several importa

103 Different alkali metal cations of the methoxide bases, however, ha

104 and the rank order of permeabilities for the alkali metal cations were unchanged.

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

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

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

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

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

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

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

112 1 in 2 days, without the need for additional alkali metal cations.

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

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

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

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

117 onformation and binding of calix[4]arenes to alkali-metal cations has been studied using a dehydroxyl

118 7.24-nm(3) cavities containing exchangeable alkali-metal cations that can be replaced by transition-

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

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

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

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

123 Under the same conditions, extraction of alkali metal chlorides into solutions of DC18C6 in chlor

124 e solvent extraction of aqueous solutions of alkali metal chlorides with solutions of dicyclohexano-1

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

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

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

128 Infrared multiphoton dissociation (IRMPD) of alkali metal-coordinated oligosaccharides was obtained i

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

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

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

132 Ion pairing of alkali metal counterions with the anionic reduction prod

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

134 uce Br(-) is almost identical for all of the alkali metal donors.

135 te density and observed superconductivity in alkali metal-doped C(60).

136 e C60 molecules follows the general trend of alkali metal-doped C60 and suggests routes to even highe

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

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

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

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

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

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

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

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

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

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

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

148 The A3C60 alkali metal fullerides are superconducting systems in w

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

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

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

152 .Li and HC6.Cs indicate that the size of the alkali metal has some influence on the conformation of c

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

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

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

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

157 This combination of alkali metal hydroxide base, H2O, and the ammonium salt

158 n the presence of inexpensive and air-stable alkali metal hydroxide bases and Pd[P(t-Bu)3]2 as cataly

159 5a-o, and 6a-e using superbasic solutions of alkali-metal hydroxides in DMSO is described.

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

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

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

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

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

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

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

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

168 Alkali metal intercalation into polyaromatic hydrocarbon

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

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

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

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

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

174 upon MALDI, whereas PES homopolymers require alkali metal ion addition to become detectable.

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

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

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

178 e the following features: (i) new motifs for alkali metal ion complexation (i.e., cationic receptors

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

180 (HC4) illustrate the great influence of the alkali metal ion on the solid state structure of calixan

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

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

183 e half-reaction kinetic parameters depend on alkali metal ion size in a manner similar to that observ

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

185 particularly sensitive method for detecting alkali metal ion-binding sites in nucleic acid crystals.

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

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

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

189 For larger alkali metal ions (K+, Rb+, and Cs+), the major products

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

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

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

193 Not only can alkali metal ions be readily located in such structures,

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

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

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

197 atures most conducive to complexation of the alkali metal ions Li(+), Na(+), and K(+) in a series of

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

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

200 The anomalous influence of alkali metal ions on the reduction current is consistent

201 The alkali metal ions serve as in situ chemical ionization r

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

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

204 The capability of 3 to coordinate to alkali metal ions was quantified.

205 There is no evidence of alkali metal ions within this spine.

206 shows no measurable tendency to complex with alkali metal ions, 3 binds strongly to Li(+) and Na(+) i

207 lectivities for Na(+), Ca(2+), Ba(2+), other alkali metal ions, and Cl(-) thus can be predicted by vo

208 he crown-TTF disulfides 7c,d,f can recognize alkali metal ions, and the process can be monitored foll

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

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

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

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

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

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

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

216 , Rb+, and Cs+), the major products were the alkali metal ions.

217 otential scans and can selectively recognize alkali metal ions.

218 assess their coordination capability toward alkali metal ions.

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

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

221 nt proline isomeric molecules complexed with alkali metal ions.

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

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

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

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

226 nspecific rather than competitive binding of alkali-metal ions.

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

228 c structures, the coordination number of the alkali metal is raised by binding of Lewis-basic solvent

229 e higher response for heavier cations of the alkali metals is consistent with the periodic trends of

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

231 roximate square planar Al(4)(2-) unit and an alkali metal led to the suggestion that Al(4)(2-) is aro

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

248 Alkali metal-oxygen batteries are of great interests for

249 ent selectivity and competitive binding with alkali metals present in solution.

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

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

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

253 e ECR-34, which can be prepared from a mixed alkali metal reaction gel containing tetraethylammonium

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

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

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

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

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

259 s(+) derived from the highly electropositive alkali metals represent prototypical charged spheres tha

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

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

262 The other alkali metal salts A(2)1 (A = Li, Na, K, Rb) precipitate

263 The alkali metal salts are not amenable for recrystallizatio

264 A complete series of X-ray structures of the alkali metal salts of calix[4]arene (HC4) illustrate the

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

266 are more conformationally flexible than the alkali metal salts of dianionic calix[6]arenes, which ha

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

268 Solution NMR spectra of alkali metal salts of monoanionic calix[4]arenes indicat

269 The alkali metal salts of monoanionic calix[6]arenes are mor

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

271 ion with twelve pendant hydroxyl groups, the alkali metal salts surprisingly displayed low water solu

272 Addition of alkali metal salts to this zirconium hydrosilazide compo

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

274 Four alkali metal salts, A(2)1 (A = Na, K, Rb, Cs), were char

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

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

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

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

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

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

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

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

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

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

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

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

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

288 Rubidium is the only other alkali metal that can replace potassium in catalyzing ty

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

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

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

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

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

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

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

296 On addition of alkali metal, we observe directly significant disruption

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

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

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

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