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1 ter by co-precipitation with barium or other alkaline earth metals.
2 ly relevant concentrations of the alkali and alkaline earth metals.
3 up of cyclohexanol and phenol with alkali or alkaline earth metals.
4 lithium attracts interest in other alkali or alkaline earth metals.
5 f the structure and electronic properties in alkaline earth metal acetylides with high-resolution mic
6 dy investigates the use of common alkali and alkaline-earth metal additives to enhance the mineraliza
7 sitive ion mode CAD with/without alkaline or alkaline earth metal adduction, the ratio of product ion
8 ormation using the d orbitals of the heavier alkaline-earth metals (Ae = Ca, Sr, Ba), the so-called "
9 r chalcogen (Se, Te) of the type AFFeAs (A = alkaline-earth metal), AFe(2)As(2), AFeAs (A = alkali me
10                                  Alkali- and alkaline-earth metal amidoboranes are a new class of com
11             Doubly charged molecular ions of alkaline earth metals and argon could be identified as s
12 ed understanding of the interactions between alkaline earth metals and DOM under conditions that are
13 The polymer does not interact with alkaline, alkaline-earth metals and transition metals.
14            The FP-APW calculations show that alkaline-earth-metal and germanium orbitals, particularl
15 e to calcium(ii) (such as the lanthanides or alkaline earth metals), and in a few key cases this targ
16 al contained higher concentrations of salts, alkaline earth metals, and organic chemicals.
17 s possessing disulfide bonds with sodium and alkaline earth metal are generated using electrospray io
18 rgan and others is that fluxes of alkali and alkaline earth metals are required for signaling, but tr
19  rigid 7 K argon matrix containing alkali or alkaline earth metal atoms and NO(2) isolated from each
20    The oxide QC formation is forced by large alkaline earth metal atoms and the reduction of their mu
21 asis for analyzing the binding of alkali and alkaline earth metal atoms over a broad range of systems
22 lery-mode microlaser scheme, where ultracold alkaline-earth metal atoms, i.e., gain medium, are tight
23 e" structure of stoichiometry AeTiO(2) (AE = alkaline earth metal, Be, Mg, Ca, Sr, and Ba), we find s
24                         Here, we report that alkaline-earth metal beryllium atoms react with OF(2) to
25                      Divalent cations of two alkaline earth metals Ca(2+) and Mg(2+) and the transiti
26 he strong binding affinity between U(IV) and alkaline earth metals (Ca(2+)/Mg(2+)/Sr(2+)/Ba(2+)), tra
27 , and all elements other than the alkali and alkaline earth metals (Ca, Mg, Sr, K, and Na) are positi
28   Our model considers perovskites containing alkaline-earth metals (Ca, Sr, and Ba) and lanthanides (
29 t actinides and rare earth metals as well as alkaline earth metals can be encapsulated within a varie
30  designing and developing 1D architecture of alkaline earth metal carbonates by a simple method witho
31  ionophore-facilitated transfer of a smaller alkaline earth metal cation with higher hydrophilicity a
32                   The structures of isolated alkaline earth metal cationized amino acids are investig
33                              The behavior of alkaline earth metal cations (Mg2+ and Ca2+) and transit
34                               In contrast to alkaline earth metal cations (Mg2+ and Ca2+), different
35 rference effects from other alkali metal and alkaline earth metal cations and has good stability and
36 est in free energy in complexes with smaller alkaline earth metal cations and that zwitterionic forms
37                    The binding of alkali and alkaline earth metal cations by macrocyclic and diazamac
38 an indeed function as ligands for alkali and alkaline earth metal cations in a manner similar to that
39 nce-dependent dsDNA condensation by divalent alkaline earth metal cations.
40  the same conclusions are valid for divalent alkaline earth metal cations.
41 tions to compare the solvation of alkali and alkaline-earth metal cations in water and liquid CO(2) a
42  as optical molecular sensors for alkali and alkaline-earth metal cations.
43 vation of singly charged cationic alkali and alkaline earth metal complexes, which results in the hig
44                                   Alkali and alkaline earth metal compounds in the dust dissolve in w
45                              Extra-framework alkaline-earth metal containing species and aluminum spe
46  The approach, based on measuring alkali and alkaline earth metal content, revealed that adulterated
47 ular complexes of the terrestrially abundant alkaline earth metals have also demonstrated promise wit
48 tal amidoborane compounds of the alkali- and alkaline earth metals have in recent years found applica
49  clathrate type-I crystals containing alkali/alkaline-earth metals have been extensively studied, but
50                                     Divalent alkaline earth metal ions condensed triple-stranded (ts)
51 model systems for understanding the roles of alkaline earth metal ions in nucleic acid processing.
52                     The effect of alkali and alkaline earth metal ions on the reactions of the cumylo
53 cated that Cd(II) and the heavier and larger alkaline earth metal ions Sr(II) and Ba(II) were effecti
54 ) among 14 different transition, alkali, and alkaline earth metal ions studied.
55                                  A series of alkaline earth metal ions was tested for the ability to
56                               Similar to the alkaline earth metal ions, application of Cd(2+) elicite
57 sequence genomic DNA, AA-TT condenses in all alkaline earth metal ions.
58 clease that prefers transition metal ions to alkaline earth metal ions.
59 resence of transition metal ions compared to alkaline earth metal ions.
60 cleavage was detected in the presence of the alkaline-earth metal ions Mg(2+), Ca(2+), Sr(2+), and Ba
61  also actively compensated by rare-earth and alkaline-earth metal ions of the interface.
62 ctivity for lead over other alkali-metal and alkaline-earth-metal ions.
63 infinite-layer compound ACuO2 (where A is an alkaline earth metal)-is an excellent way of investigati
64     The unique optical cycling efficiency of alkaline earth metal-ligand molecules has enabled signif
65 robe is selective for Hg(II) over alkali and alkaline earth metals, most divalent first-row transitio
66 ite general phenomenon: among the alkali and alkaline earth metals, Na and Mg generally have the weak
67                       Herein, we present the alkaline earth metal nitridophosphate oxide Ba(3)[PN(3)]
68 ither a preferential accumulation of heavier alkaline earth metals nor core-shell structures in the c
69 eolites, by incorporation of extra-framework alkaline-earth metals or by demetalation with dealuminat
70 daries in highly ionic materials such as the alkaline earth metal oxides and alkali halides.
71 ing solid CO(2) sorbents based on alkali and alkaline earth metal oxides operating at medium to high
72 ntial clusters with a planar hypercoordinate alkaline-earth metal (phAe) as the lowest-energy form.
73           The calculations also predict that alkaline-earth metal-porphyrin COFs could catalyze the d
74                      Alloys of platinum with alkaline earth metals promise to be active and highly st
75                                    Recently, alkaline-earth metal Sr intercalated Bi2Se3 has been rep
76 e gas wells generally yield HFFF enriched in alkaline earth metals such as Sr and Ba, known to cause
77  the presence of secondary metal ions, e.g., alkaline earth metals, transition metals, lanthanide met
78    This indicated that fractionation between alkaline earth metals was not inherent to intracellularl
79 as facilitated through the use of alkali and alkaline-earth metals, which selectively fill the availa
80 own SHG active AMCO3F (A = alkali metal, M = alkaline earth metal, Zn, Cd, or Pb) materials indicates