ライフサイエンスコーパス: ytterbium

1 both using spin-polarized, ultracold atomic ytterbium.

2 2 in the presence of calcium, strontium, and ytterbium.

3 is presented of significant covalency in the ytterbium 4f shell of tris-cyclopentadienyl ytterbium (Y

4 Reaction of calcium or ytterbium amalgam with [CpFe(CO)(2)](2) (Fp(2)) gave the

5 tion coefficients between samarium and 57Fe, ytterbium and 58Fe, and dysprosium and 54Fe were 0.992,

6 -electron intermetallic compounds of cerium, ytterbium and various 5f elements bridges the extremes,

7 rbium, dysprosium, holmium, erbium, thulium, ytterbium, and lutetium), and gold, use in the 2013 mode

8 The paramagnetic europium, ytterbium, and praseodymium complexes Li 3(THF) n (BINOL

9 t is, 100 kVp and higher-barium, gadolinium, ytterbium, and tantalum provided consistently increased

10 he available high-energy kHz-repetition-rate Ytterbium-based laser amplifiers (delivering 180-fs, 103

11 A novel ytterbium binding site is also found at the dimer two-fo

12 d strontium bind in the same location, while ytterbium binds several angstroms removed.

13 riarylmethanes bearing secondary anilines by ytterbium-catalyzed Friedel-Crafts reaction of hetero(ar

14 The ytterbium complex with the crown is suitable for use in

15 The divalent calcium and ytterbium compounds M(C(SiHMe(2))(3))(2)THF(2) contain b

16 A phospholipid chelate complexed with ytterbium (DMPE-DTPA:Yb3+) is shown to be readily incorp

17 crolaser by free-space optical pumping of an Ytterbium doped silica microtoroid via the scatterers.

18 Partial ytterbium f-orbital occupancy (i.e., intermediate valenc

19 luding iodine, barium, gadolinium, tantalum, ytterbium, gold, and bismuth, were formulated as compoun

20 Evidence indicates that the ytterbium(III) bonds to the carboxylic acid moieties of

21 from the various AuNP conjugates to pendant ytterbium(III) cations, a Dexter-type energy transfer me

22 capped gold nanoparticles (AuNPs) to pendant ytterbium(III) cations.

23 )-2,3,11,12-tetracarboxylic acid (I) and its ytterbium(III) complex are evaluated as chiral NMR discr

24 energy transfer process, the distance of the ytterbium(III) from the surface of the AuNPs is systemat

25 Addition of ytterbium(III) nitrate to crown-substrate mixtures cause

26 adily accessible ynamides in the presence of ytterbium(III) trifluoromethanesulfonate [Yb(OTf)3], N-i

27 hile the signal appears at the transition of ytterbium ion ((171)Yb(+), 369.5 nm) and the idler appea

28 A quantum bit stored in a single trapped ytterbium ion (Yb+) is teleported to a second Yb+ atom w

29 ous difference Fourier map revealed that two ytterbium ions (Yb(3+)) could bind the catalytic site of

30 nteraction between the AuNP ligand shell and ytterbium is determined using both nuclear magnetic reso

31 onfigurational, open-shell singlets in which ytterbium is intermediate valent.

32 Ytterbium metal reacts with PhEEPh (E = S, Se, Te) and e

33 equivalent amounts of 58Fe-labeled iron and ytterbium; on day 3, a well-absorbed reference dose of 5

34 erent stable isotopes of iron with samarium, ytterbium, or dysprosium.

35 is material has a three-dimensional cationic ytterbium oxyhydroxide framework with one-dimensional ch

36 absorption of the chromophore compared with ytterbium's intrinsic absorption.

37 mospecifically activated upon treatment with ytterbium triflate and N-iodosuccinimide and (b). coupli

38 compound, 6, in the presence of scandium or ytterbium triflate in 1,2-dichloroethane or a cosolvent

39 Substoichiometric quantities of scandium and ytterbium triflate increase the yield of Ugi four compon

40 In the presence of ytterbium triflate, in the cosolvent system, the reactio

41 orated by formation of the silyl enol ether, ytterbium triflate-catalyzed condensation with formaldeh

42 by iodonium ion, specifically generated from ytterbium triflate/N-iodosuccinimide, can be used to mon

43 Scandium and ytterbium triflates respond very differently to these do

44 um trifluoromethanesulfonate (Y(OTf)(3)) and ytterbium trifluoromethanesulfonate (Yb(OTf)(3)).

45 Data used to support this claim include ytterbium valence measurements using Yb L(III)-edge X-ra

46 s completely unoccupied while the low-energy ytterbium (Yb) 4f states become increasingly itinerant,

47 We demonstrate a ytterbium (Yb) and an erbium (Er)-doped fiber laser Q-sw

48 This makes ytterbium (Yb)-169, which emits photons with an average

49 ytterbium 4f shell of tris-cyclopentadienyl ytterbium (YbCp(3)) in its electronic ground state, that