ライフサイエンスコーパス: lanthanide

1 ttice strain effects induced by changing the lanthanide.

2 pass mid-range oxidation state actinides and lanthanides.

3 h a focus on the separation of actinides and lanthanides.

4 AuNPs with the narrow emissive properties of lanthanides.

5 r masses of material, including high-opacity lanthanides.

6 terfering cations and anions, especially the lanthanides.

7 with the relatively short-lived emission of lanthanides.

8 ces between the complexes of Am(III) and the lanthanides.

9 ich Ln-MB wheels for effective separation of lanthanides.

10 due to the similar coordination chemistry of lanthanides.

11 uctures upon binding to metal centers and/or lanthanides.

12 with multiple ejecta components of differing lanthanide abundance.

13 e metals" yet much remains unknown regarding lanthanide acquisition and homeostasis.

14 manipulate energy migration within the same lanthanide activator ion (Er(3+)) towards orthogonal red

15 This is the first time that the amidato lanthanide amides ({L (n)Ln[N(SiMe(3))(2)]THF}(2) ( n =

16 even more pronounced in gadolinium, curium's lanthanide analogue, owing to the contraction of the 4f

17 In comparison with lanthanide analogues, significant d- and f-electron cont

18 Given the very basics of lanthanide and actinide chemistry are being frequently r

19 iscrimination of heavy metal ions, including lanthanide and actinide salts in aqueous solution.

20 xhibiting high valence states such as in the lanthanide and actinide series.

21 ntonites allows them to immobilize trivalent lanthanide and actinides in the environment.

22 have studied the ORR on eight platinum (Pt)-lanthanide and Pt-alkaline earth electrodes, Pt5M, where

23 Lanthanides and actinides are elements of ever-increasin

24 as 70 nM, and highly similar metals such as lanthanides and actinides can be easily distinguished at

25 The behavior of the f-electrons in the lanthanides and actinides governs important macroscopic

26 ted periodic trends for hydration across the lanthanides and distinguish complexes with several inner

27 iate between that observed for the trivalent lanthanides and for the transition metals.

28 and influx of extracellular Ca(2+) Although lanthanides and Gsdmd deletion both suppressed PM pore a

29 c(III) reactivity is often inferred from the lanthanides and minor actinides (that is, Am, Cm), with

30 ndamental chemical incompatibilities between lanthanides and most intermediate-gap semiconductors.

31 Lanthanides and other microelements were then used for d

32 the rare earth elements (REEs) together with lanthanides and scandium.

33 -66 series, which includes transition metal, lanthanide, and early actinide elements in the hexanucle

34 The chemistry encompasses transition metals, lanthanides, and actinides and describes recently discov

35 ic configurational entropy is sizable in all lanthanides, and reaches a maximum value of approximatel

36 y chemical differences between actinides and lanthanides-and between different actinides-can be ascri

37 scandium, yttrium and the series of fifteen lanthanides are an intriguing family of MOFs from the st

38 e separation of the minor actinides from the lanthanides are critical to the closure of the nuclear f

39 ol sensitivity in the fae mutant strain when lanthanides are present, providing evidence for the capa

40 Lanthanides are routinely incorporated into quantum dots

41 ent developments in the understanding of how lanthanides are selectively acquired and used by certain

42 ion electron microscopy, we demonstrate that lanthanides are stored as cytoplasmic inclusions that re

43 lipids-based internal standard, and a spiked lanthanide as a secondary internal standard.

44 The distribution of lanthanides as determined by means of ICP-MS analysis ap

45 tion times have been demonstrated for single lanthanide atoms in molecular magnets, for lanthanides d

46 morphism is the general behavior for typical lanthanide based metallic glasses.

47 mass cytometry and reduces interference with lanthanide-based antibody measurement.

48 Lanthanide-based dinitrogen reduction chemistry has been

49 In this work, we present a novel lanthanide-based luminescent metal-organic framework, na

50 Here, we report a series of lanthanide-based MOFs that allow fine tuning of the shee

51 Our results allow the development of lanthanide-based optical clocks with a relative uncertai

52 This work demonstrates that lanthanide-based paramagnetic shift reagents can be desi

53 Lanthanide-based point defects, such as trivalent ytterb

54 anges of the Nav voltage sensor domain using lanthanide-based resonance energy transfer (LRET) betwee

55 l architectural details of BK channels using lanthanide-based resonance energy transfer (LRET).

56 , we confirmed its binding to Nav1.4 through Lanthanide-based Resonance Energy Transfer.

57 in magnetic resonance imaging in the 1980s, lanthanide-based small molecules and nanomaterials have

58 of physical properties have been explored in lanthanide-bearing borohydrides related to solid state p

59 alizing the OmpA protein with 16 copies of a lanthanide binding tag (LBT).

60 through high-density cell surface display of lanthanide binding tags (LBTs) on its S-layer.

61 We previously engineered E. coli to express lanthanide binding tags on the cell surface, which incre

62 self-assembled monolayers (SAMs) of helical lanthanide-binding peptides.

63 We present a covalent paramagnetic lanthanide-binding tag (LBT) for increasing the chemical

64 We used a genetically encoded lanthanide-binding tag (LBT) to bind terbium as a LRET d

65 ed by the inclusion of an encoded N-terminal lanthanide-binding tag (LBT), and LRET between the lumin

66 We report the application of lanthanide-binding tags (LBTs) for two- and three-dimens

67 ed donor constructs with genetically encoded lanthanide-binding tags (LBTs) inserted at the extracell

68 coli strain previously engineered to display lanthanide-binding tags on the cell surface was encapsul

69 ave surged as materials of choice for doping lanthanides, but they have non-negligible shortcomings i

70 indium, and bismuth in addition to the four lanthanides) by multistage dispersion polymerization for

71 e subtle bonding differences among trivalent lanthanides can be amplified during the crystallization

72 such alkenes catalyzed by iridium, gold, and lanthanide catalysts are known, but they have required a

73 The lanthanide-catalyzed oxidative C-O coupling of 1,3-dicar

74 lysis of a series of [Ln(Cp(ttt))2](+) (Ln = lanthanide) cations could shed light on these properties

75 nation of the phenacyl carbonyl group to the lanthanide center.

76 The highest lanthanide-centered luminescence quantum yields were 35%

77 onspecific interactions of multiple unstable lanthanide chelates and nonantenna ligands with sample l

78 onspecific interactions of multiple unstable lanthanide chelates and selected chemicals within the sa

79 ady described ligand L(4a), two pyclen-based lanthanide chelators, L(4b) and L(4c), bearing two speci

80 variety of different reaction mechanisms in lanthanide chemistry appear to be broader than the simpl

81 we characterize trefoil-shaped outer-sphere lanthanide chloride and nitrate ion clusters in hydrocar

82 A lanthanide cluster, PCC-72, which is the second largest,

83 This model lanthanide complex has two open coordination sites that,

84 r granny and square knots through the use of lanthanide-complexed overhand knots of specific handedne

85 al design of more effective photoluminescent lanthanide complexes are discussed.

86 Lanthanide complexes are of increasing importance in can

87 question, and likely for a large fraction of lanthanide complexes in general.

88 er underscoring the value and versatility of lanthanide complexes in homogeneous catalysis.

89 ligand field splitting-does not hold for the lanthanide complexes in question, and likely for a large

90 The photo-induced dissociative-ionization of lanthanide complexes Ln(hfac)(3) (Ln = Pr, Er, Yb) is st

91 Cyanide ions are shown to interact with lanthanide complexes of phenacylDO3A derivatives in aque

92 The lanthanide complexes of these ligands were investigated

93 etic NMR shifts in a series of isostructural lanthanide complexes relavant to PARASHIFT contrast agen

94 By contrast, lanthanide complexes with DOTAM derivatives display no a

95 properties, yet such studies on multinuclear lanthanide complexes with strong magnetic coupling remai

96 o closely related series of eight-coordinate lanthanide complexes, a switch in the sign of the domina

97 etween QDs and fluorescent dyes, luminescent lanthanide complexes, and bioluminescent proteins.

98 [S2 P((t) Bu2 C12 H6 )]4 and two isomorphous lanthanide complexes, namely one with a similar ionic ra

99 Organometallic lanthanide compounds first gave a tantalizing glimpse of

100 MAPq utilizes lanthanide-conjugated antibodies to simultaneously quant

101 We demonstrate how the lanthanide contraction can be used to control strain eff

102 The lanthanide contraction was employed to systematically va

103 it in its structure, as a consequence of the lanthanide contraction.

104 In this study, we report a probe of lanthanide-coordinated semiconducting polymer dots (Pdot

105 ated the functional importance of a proposed lanthanide-coordinating aspartate residue.

106 e a strategy to develop efficient and stable lanthanide coordination polymers (LCPs) with tunable lum

107 bioprobe, which, depending on the complexed lanthanide, could be used in various applications.

108 transuranium actinide ions and their lighter lanthanide counterparts are of fundamental importance fo

109 methanol dehydrogenase (MDH) shifts from the lanthanide-dependent MDH (XoxF)-type, to the calcium-dep

110 ethylorubrum extorquens AM1, the periplasmic lanthanide-dependent methanol dehydrogenase XoxF1 produc

111 bits calcium-dependent, and as we show here, lanthanide-dependent methanol dehydrogenases, which are

112 opy techniques were used to characterize the lanthanide deposited layer.

113 The lanthanide derivatives were fully characterized using (1

114 e lanthanide atoms in molecular magnets, for lanthanides diluted in bulk crystals, and recently for e

115 Nitrogenous bases, thiols, and lanthanides do not interfere in the fluorometric detecti

116 rocess between the diarylethene acceptor and lanthanide donor, resulting in reversible luminescence o

117 three-dimensional distribution of aliovalent lanthanide dopants in ceria catalysts and their effect o

118 ntrol is vital for designing multifunctional lanthanide-doped core/shell nanocrystals.

119 et dynamics by coupling organic molecules to lanthanide-doped inorganic insulating nanoparticles.

120 opant concentration to less than 1-5 mol% in lanthanide-doped materials, and this remains a major obs

121 Herein we report a new class of contracted lanthanide-doped MB structures that have replaced all th

122 n and surface quenching effects in colloidal lanthanide-doped nanocrystals, and that inert epitaxial

123 enhance the photon upconversion processes in lanthanide-doped nanocrystals.

124 Here, we synthesize small lanthanide-doped nanoparticles and measure the absolute

125 ch nanomaterials is represented by colloidal lanthanide-doped semiconductor nanocrystals (LnSNCs).

126 hods were applied to the characterization of lanthanide-doped upconversion nanoparticles (UCNPs) by S

127 Lanthanide-doped upconversion nanoparticles (UCNPs) have

128 pment of liquid marbles coated with magnetic lanthanide-doped upconversion nanoparticles (UCNPs) that

129 Zn(2+) fluorescent-based probe by assembling lanthanide-doped upconversion nanoparticles (UCNPs) with

130 Lanthanide-doped upconversion nanoparticles are particul

131 Lanthanide-doped upconverting nanoparticles (UCNPs) have

132 ere, we present a new strategy for accessing lanthanide-doped visible-light-absorbing semiconductor n

133 Similarly, 2 exhibits an elliptical lanthanide-doped wheel {Mo120 Ce6 } that is sealed by a

134 We explore UCNP composition, size, and lanthanide doping-dependent emission, focusing on upconv

135 h different atomic weight ratio (R) of Fe to Lanthanide (Dy + Tb) using electron beam co-evaporation

136 Alloys simulating the formation of the lanthanide element Nd within U-Zr-Te are also evaluated,

137 of commercially available beads carries four lanthanide elements (cerium, europium, holmium, and lute

138 The lanthanide elements (Ln(3+)), those with atomic numbers

139 Lanthanide elements have been recently recognized as "ne

140 f these surface-confined macrocycles to host lanthanide elements is assessed, introducing a novel off

141 ng Fe (66 atomic (at.) %) along with the two Lanthanide elements Tb (10 at.%) and Dy (24 at.%) can sh

142 ersible luminescence on-off switching of the lanthanide emitting center in the MOF host.

143 nd a prerequisite of data storage-and so far lanthanide examples have exhibited this phenomenon at th

144 between orbital and spin angular momenta in lanthanide f orbitals.

145 "Lanthanides find extensive applications in displays, mag

146 fuels primarily due to interactions between lanthanide fission products and cladding constituents.

147 ng, separating trivalent minor actinides and lanthanide fission products is extremely challenging and

148 tential additive for U-Zr fuels to bind with lanthanide fission products, e.g. neodymium (Nd), negati

149 It includes the chemical separation of lanthanides, followed by the preparation of proper sampl

150 ation procedure was developed to isolate the lanthanide fraction and to prepare thin samples for alph

151 are spurring interest in the development of lanthanide-free hard magnets.

152 s the blue component requires high-velocity, lanthanide-free material.

153 Lanthanides have been investigated extensively for poten

154 As the lanthanides have high coordination requirements, their u

155 Chromium lanthanide heterometallic wheel complexes {Cr8 Ln8 } (Ln

156 Lanthanide hexaborides (LnB(6) ) have disparate and ofte

157 se of the NIR emission arising from a single lanthanide(III) cation for optical biological imaging of

158 Through the appropriate choice of lanthanide(III) cations, the same reactive ligand can be

159 the highest NIR quantum yield reported for a lanthanide(III) complex containing C-H bonds with a valu

160 ain challenge in the creation of luminescent lanthanide(III) complexes lies in the design of a ligand

161 oward versatile, easily prepared luminescent lanthanide(III) complexes suitable for a variety of appl

162 We report first prototypes of responsive lanthanide(III) complexes that can be monitored independ

163 ent dependence of NMR shifts for a series of lanthanide(III) complexes, namely [LnL(1)] (Ln = Eu, Tb,

164 de) oligomer with six chiral centers using a lanthanide(III) ion template.

165 Single lanthanide(III) ion white light emission is in high dema

166 y and is able to sensitize several different lanthanide(III) ions emitting in the visible and/or in t

167 The use of lanthanide(III) ions of different natures for these imag

168 Luminescence of lanthanide(III) ions sensitively reflects atomic environ

169 ligands able to separate actinide(III) from lanthanide(III) metal ions in view of the treatment of t

170 Luminescent lanthanide(III)-based molecular scaffolds hold great pro

171 oton excitation, (ii) the first example of a lanthanide(III)-based NIR-emitting probe that can be tar

172 stereoinduction: in the case of one knot, a lanthanide(III)-coordinated crossing pattern formed only

173 ICP-MS absolute quantification of the lanthanide in the printed layer ensured the reproducibil

174 ctive separation of trivalent actinides from lanthanides in biphasic solvent systems.

175 role of microelements and, in particular, of lanthanides in the oil production chain has been studied

176 As the potential utility of lanthanides in these areas continues to increase, this t

177 n differs from Ln(NR2 )3 reactions (Ln=Y and lanthanides) in that it occurs under N2 without formatio

178 a TonB-ABC transport system is required for lanthanide incorporation to the cytoplasm.

179 Lanthanide-induced pseudocontact shifts are demonstrated

180 Alignment of the helix by a paramagnetic lanthanide ion attached to its N-terminal region shows a

181 . 15-20 amino acids) affording high-affinity lanthanide ion binding, and X-ray fluorescence microscop

182 The oligomer folds around the lanthanide ion to form an overhand knot complex of singl

183 Typical transition metal ion Mn(2+) and lanthanide ion Yb(3+) are adopted as a case study via th

184 tile chemical and magnetic properties of the lanthanide-ion 4f electronic configuration.

185 Herein some examples of the use of lanthanide ions (f-metal ions) to direct the synthesis o

186 We used lanthanide ions (Ln(3+)) as probes to investigate the Ca

187 rials for sensitizing near-infrared emitting lanthanide ions (Ln(3+)) for biological imaging, long-wa

188 zine-2,4,6-triyltribenzoate (TATB) and mixed lanthanide ions (Tb(3+) and Eu(3+)).

189 Transition metals and lanthanide ions display unique characteristics (i.e., ma

190 ng, demonstrating that magnetic, tetravalent lanthanide ions engage in covalent metal-ligand bonds.

191 cant implications for the use of tetravalent lanthanide ions in magnetic applications since the obser

192 for further extending the known tetravalent lanthanide ions in molecular complexes.

193 metallated them with various transition and lanthanide ions in the fluorous phase.

194 Doping lanthanide ions into colloidal semiconductor nanocrystal

195 pectrally narrow, long-lived luminescence of lanthanide ions makes optical nanomaterials based on the

196 This allows the lanthanide ions necessary for stabilizing the entangled

197 hat have replaced all the {Mo(2)} units with lanthanide ions on the inner rim, giving the general for

198 lecular strand by using transition-metal and lanthanide ions to guide chain folding in a manner remin

199 pairs, these particles contain many emitting lanthanide ions together with numerous acceptor dye mole

200 molecules can undergo energy transfer to the lanthanide ions with unity efficiency, which allows us t

201 The protein binds lanthanide ions with very high affinity as demonstrated

202 anical description of optical transitions in lanthanide ions, and their influence on laser cooling.

203 ot of single handedness upon coordination to lanthanide ions, both in isotropic solutions and in liqu

204 When doped with lanthanide ions, both ScOOH and Sc2 O3 can be utilized f

205 Among the tetravalent lanthanide ions, only Ce(4+) forms stable coordination c

206 llisecond-scale luminescence lifetime of the lanthanide ions, was applied to fixed T24 cancer cells u

207 nt thermometer based on the emissions of two lanthanide ions.

208 al sensitization and energy transfer between lanthanide ions.

209 exploiting the synergy between coordinating lanthanides ions as symmetry breakers to produce MBs wit

210 r light absorption intrinsically featured by lanthanides is compensated by the semiconductor moiety,

211 nding of the minor actinides (Am, Cm) versus lanthanides is key for developing advanced nuclear-fuel

212 we developed a series of protease-selective lanthanide-labeled probes compatible with mass cytometry

213 Structurally authenticated, terminal lanthanide-ligand multiple bonds are rare and expected t

214 and on a new strategy for isolating terminal lanthanide-ligand multiple bonds using cerium(IV) comple

215 Lanthanide (Ln(3+)) doping in alumina has shown great pr

216 sensors for Gsp using near-infrared emitting lanthanide (Ln(3+)) materials, including Ln(3+) MOFs and

217 Luminescent lanthanide (Ln(III)) complexes with coumarin or carbosty

218 (FRET) between fluorescent dyes and between lanthanide (Ln) complexes and dyes that hybridize to bet

219 Lanthanide (Ln) elements are utilized as cofactors for c

220 Lanthanide (Ln) group elements have been attracting cons

221 Out of the 14 lanthanide (Ln) ions, molecular complexes of Ln(IV) were

222 Monazite is a naturally occurring lanthanide (Ln) phosphate mineral [Ln (x) (PO(4) ) (y) ]

223 Recently, rare-earth elements lanthanides (Ln(3+) ) have emerged as enzyme cofactors o

224 Lanthanides (Ln(3+)) are critical materials used for man

225 Lanthanides (Ln) usually occur in the +3, or more recent

226 Cluster chemistry involving Y, lanthanides (Ln, from La to Lu), actinides (An, from Ac

227 n the field have demonstrated that trivalent lanthanide, Ln(III), incorporated into ZnAl(2)O(4) spine

228 ion of rare earth elements (REEs), including lanthanides (Lns), would facilitate mining and recycling

229 on electron microscopy was used to visualize lanthanide localization.

230 en synthesized, to form a complete family of lanthanide luminescent bioprobes: [EuL(4a)], [SmL(4a)],

231 in just 5.3 min and locate individual 15 mum lanthanide luminescent microspheres with standard deviat

232 a electrons and should exist for a series of lanthanide M(III) [eta(7) -B7(3-) ] complexes.

233 amide ligands (1) with point chirality about lanthanide metal ion (Ln(3+)) templates, in which the he

234 ed for the C-O coupling process in which the lanthanide metal ion serves as Lewis acid to activate th

235 otoswitchable diarylethene derivative into a lanthanide metal-organic framework (MOF).

236 Seven isomorphous lanthanide metal-organic frameworks in the PCMOF-5 famil

237 In this work, a series of mixed lanthanide metal-organic frameworks were synthesized usi

238 Our results highlight the versatility of lanthanide metallocenophane architectures toward the dev

239 The first example of a lanthanide metallocenophane complex has been isolated as

240 m material comprising of transition (Fe) and Lanthanide metals (Dy and Tb) that show unique combinati

241 s methodology to label oligonucleotides with lanthanide metals for use in mass cytometry.

242 By tuning the lanthanide metals in mixed-metal lanthanide MOFs and by

243 gues A1-x B x MnO3 (A and B = main group and lanthanide metals) are a fascinating family of magnetic

244 y alloy systems consisting of transition and lanthanide metals.

245 in methane by bis(permethylcyclopentadienyl)lanthanide methyl [(eta(5) -C5 Me5 )2 Ln(CH3 )] complexe

246 tuning the lanthanide metals in mixed-metal lanthanide MOFs and by using the organic linkers as ante

247 e that the triplet excitons generated in the lanthanide nanoparticle-molecule hybrid systems by near-

248 dictions that Bi1-xRxFeO3 systems (R being a lanthanide, Nd in this work) can potentially allow high

249 ogous to that of the isostructural trivalent lanthanide-only containing material GWMOF-6.

250 ontrolled by two parameters: acidity and the lanthanide or transition-metal countercation.

251 lose resemblance to calcium(ii) (such as the lanthanides or alkaline earth metals), and in a few key

252 to yield molecular complexes of high-valent lanthanides, other than the ubiquitous Ce(4+) ion, are e

253 g organic layers into a 3D framework through lanthanide-oxygen chains.

254 Lanthanide permanent magnets are widely used in applicat

255 colloidal synthesis of intrinsically chiral lanthanide phosphate nanocrystals, measured via circular

256 This novel mixed-lanthanide polyMOF membrane exhibits not only the integr

257 tion (X Solution or X SOL), characterized by lanthanide polyoxometalates (LnPOMs) as heavy atoms sour

258 Lanthanides possess similar chemical properties renderin

259 The close spatial inter-lanthanide proximity, in combination with mu2-bridging s

260 t magnetic monopoles should exist in several lanthanide pyrochlore magnetic insulators(5,6), includin

261 f REE was low from the monazite with maximal lanthanide release reaching >40 mg L(-1) , leached REE w

262 irst examples within this large family where lanthanides replace the atoms of a main group element.

263 criptional reporter fusions show that excess lanthanides repress the gene encoding the TonB-receptor.

264 t rapidly becomes red, and a higher-opacity, lanthanide-rich ejecta component may contribute to the e

265 The vast range of lanthanide salts (La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho

266 It is shown that lanthanide salts may be used in combination with peroxid

267 Bis-cyclopentadienyl lanthanide sandwich complexes have emerged as the leadin

268 t pH control in TALSPEAK (Trivalent Actinide-Lanthanide Separation by Phosphorus reagent Extraction f

269 most popular assumptions about isostructural lanthanide series is wrong.

270 ferrites, where R is a rare-earth ion of the lanthanide series, are attracting attention mostly becau

271 d under identical reaction conditions across lanthanide series, further leading to an efficient and c

272 ed as a more sensitive tool to recognize the lanthanide signal and assign underlying electronic trans

273 es, which reveal this system to be the first lanthanide SMM in which all low-lying Kramers doublets c

274 ocesses operating in bis-C(5)/C(4)P sandwich lanthanide SMMs, which is the necessary first step towar

275 rin ligand, as induced by a protein-attached lanthanide spin label, provided structural restraints fo

276 This area of lanthanide supramolecular chemistry is fast growing, tha

277 sformed by a variety of transition metal and lanthanide systems.

278 Because mass cytometry uses a set of lanthanide-tagged antibodies, each being specific for a

279 In this report, we used lanthanide-tagged isotypes, which allowed for correction

280 rements of pseudocontact shifts generated by lanthanide tags attached to the protein, which in turn a

281 e and electronic properties of actinides and lanthanides that are difficult to synthesize or characte

282 , providing chemical recognition of specific lanthanides that originates from Ln(3+) coordination alt

283 h those found for Am(III), Cf(III), and with lanthanides that possess similar ionic radii.

284 After separation of the lanthanides, the molecular plating technique was applied

285 lthy tissues; second is the use of trivalent lanthanides to treat osteoporosis, an emerging concept w

286 useful for identification and assignment of lanthanide transitions and increases the potential of fl

287 Lanthanide transport and trafficking genes were also ide

288 re measured using strains lacking individual lanthanide transport cluster genes, and transmission ele

289 sis, robust IL-1beta release was observed in lanthanide-treated BMDMs but not in Gsdmd-deficient cell

290 Lanthanide triflates have been used to incorporate Nd(II

291 ion can undergo efficient upconversion via a lanthanide-triplet excitation fusion process: this proce

292 nversion emission and relatively short-lived lanthanide upconversion emission in a particulate platfo

293 Growth and lanthanide uptake were measured using strains lacking in

294 inescent) and coordination properties of the lanthanides, which are often transferred to the resultin

295 tional information on the interaction of the lanthanide with the sugar component was provided by meas

296 Americium and Cm were separated from the lanthanides with over 99.9% completion.

297 significantly between complexes of different lanthanides with the same ligand: one of the most popula

298 HF)x]2[mu-eta(2):eta(2)-N2] (Ln = Sc, Y, and lanthanides; x = 0, 1; A = anionic ligand such as amide,

299 total REE content (defined as the sum of the lanthanides, yttrium, and scandium) for ashes derived fr

300 ments (REEs, herein defined as the 14 stable lanthanides, yttrium, and scandium).