ライフサイエンスコーパス: polyatomic

1 eting complex vibrational spectra for larger polyatomic adsorbates.

2 cohol- and amine-functionalized amino acids, polyatomic anionic sulfur species, NO, and HNO.

3 We describe the use of polyatomic anions for the quantitative assembly of ion-p

4 on acceptor aromatic compound, with mono- or polyatomic anions switches from the almost exclusive for

5 The complexation of bidentate polyatomic anions that are complementary in size and sha

6 or determining low concentrations of aqueous polyatomic anions using attenuated total reflectance (AT

7 ve combined new studies of the reactivity of polyatomic anions, acetate, trifuoroacetate, cyanide, an

8 sporters exchange H+ for halides and certain polyatomic anions, but exclude cations, F-, and larger p

9 iteria apply for electron transfer involving polyatomic anions.

10 In contrast, this polyatomic cation finds long-lived conformational states

11 h soft and reactive landing of mass-selected polyatomic cations and anions.

12 y (SERS) was used to detect and characterize polyatomic cations and molecules that were electrospraye

13 low for the presence of functional groups in polyatomic crystal structures, and test the formula agai

14 Our results point to polyatomic crystals as promising hosts for coherent qubi

15 ronegative elements in such compounds form a polyatomic electron-accepting molecule inside the solid,

16 In this study, a completely new way of polyatomic interference removal in ICPMS for detection o

17 High mass resolution allows polyatomic interferences at Fe masses to be resolved (es

18 rements at medium spectral resolution remove polyatomic interferences for some difficult elements lik

19 sed for all measurements in order to resolve polyatomic interferences on Si and P isotopes.

20 sed for all measurements in order to resolve polyatomic interferences on Si isotopes.

21 ffective chemical separation of isobaric and polyatomic interferences prior to sample introduction.

22 tion, while for the chromatographic analyses polyatomic interferences were minimized by the use of a

23 For the former two cases polyatomic interferences were resolved by operating the

24 nalyte ions ((31)P, (32)S, and their on-mass polyatomic interferences).

25 ctral interferences, isobaric interferences, polyatomic interferences, and abundance sensitivity prob

26 s of analysis for masses with O- and N-based polyatomic interferences.

27 ing isotope ratios examined for isobaric and polyatomic interferences.

28 ifferences were observed between samples for polyatomic ion and amino acid concentrations.

29 The introduction of polyatomic ion beams, particularly C60, for TOF-SIMS ana

30 The introduction of polyatomic ion beams, such as C(60), has provided the as

31 This polyatomic ion has been tentatively identified as HSO3+

32 A polyatomic ion is observed on mass 81 in a synthetic sul

33 anic systems is demonstrated against another polyatomic ion source (e.g., SF(5)(+)).

34 Polyatomic ions and neutrals larger than a triatomic pla

35 Ambient ion soft landing, a process in which polyatomic ions are deposited from air onto a surface at

36 Polyatomic ions are observed on masses 79 and 81 in a sy

37 These polyatomic ions do not interfere with the detection of b

38 These polyatomic ions have been tentatively identified as PO3+

39 leaves, and chemical data were obtained for polyatomic ions, amino acids, sugars and organic acids.

40 er UV-absorbing groups in a variety of large polyatomic ions.

41 r the controlled deposition of mass selected polyatomic ions.

42 The polyatomic model of CF4(aq) studied gives a satisfactory

43 he retrieval of multiple bond lengths from a polyatomic molecule by simultaneously measuring the C-C

44 eter to mole ratios is complicated because a polyatomic molecule containing enriched atoms will resul

45 ements, the reaction dynamics of a prototype polyatomic molecule such as CH4 (and isotopologues) in i

46 ts properties within the context of a floppy polyatomic molecule.

47 molecular hydrogen, H(3)(+), is the simplest polyatomic molecule.

48 rational Stark-associated phenomena of small polyatomic molecules are modelled using extensive spectr

49 and associated radiation damage of atoms in polyatomic molecules can be inferred from the charge tha

50 nt studies suggest that the DIB carriers are polyatomic molecules containing carbon.

51 should be routinely considered when studying polyatomic molecules in intense laser fields.

52 the breaking and making of chemical bonds in polyatomic molecules is poised to open new pathways for

53 iate and observe such electronic dynamics in polyatomic molecules represents a crucial step forward i

54 necessary in order to assign spectra of hot polyatomic molecules such as water.

55 show that the femtosecond response of small polyatomic molecules that contain one heavy atom to ultr

56 ic generation and strong-field ionization in polyatomic molecules undergoing bonding or configuration

57 ge ultrafast structural changes in gas-phase polyatomic molecules with sub-Angstrom spatial and femto

58 In polyatomic molecules, however, the electronic states are

59 le (about 4 electron volts) are reported for polyatomic molecules, including (CH3)2CO (acetone), CH3C

60 reconstructing two-dimensional structure of polyatomic molecules.

61 ion barrier) in the mechanical activation of polyatomic molecules.

62 nts in the atomic manipulation of individual polyatomic molecules.

63 l coupled electronic and nuclear dynamics in polyatomic molecules.

64 nic, rotational, and vibrational energies of polyatomic molecules.

65 nce of tunneling to the surface diffusion of polyatomic organic molecules.

66 (+) should be thought of as covalently bound polyatomic precursors or fragments that can react and be

67 attributed to the sputter characteristics of polyatomic primary ion bombardment (SF5+) as compared to

68 dary ion mass spectrometry employing an SF5+ polyatomic primary ion source was utilized to obtain a s

69 pectrometry (cluster SIMS) employing an SF5+ polyatomic primary ion sputter source in conjunction wit

70 This study shows that polyatomic primary ions can be used for the molecular de

71 depth and high sputter rates obtained using polyatomic primary ions have facilitated their use for t

72 generated by impacts of the kiloelectronvolt polyatomic primary ions on NaNO3 were markedly different

73 he depth profiling of polymer surfaces using polyatomic primary ions.

74 coincidence counting allowed the atomic and polyatomic projectile impacts on a particular sample sur

75 eaks produced by the kiloelectronvolt energy polyatomic projectile impacts on NaNO2 were NO2- and Na(

76 omer abundance can be increased by using the polyatomic projectile ReO4- (approximately 5 keV).

77 ear dynamics that make up a multidimensional polyatomic reaction coordinate.

78 of the dynamics of elementary (bimolecular) polyatomic reactions in the gas-phase have occurred.

79 uding those reported in this work, for these polyatomic reactions.

80 he proximal distributions evaluated here for polyatomic solutes accurately reconstruct the observed d

81 by the endothermic chemical reactions of the polyatomic species inside the collapsing bubble.

82 ule, so many other molecular ions, including polyatomic species, could be treated using the same meth

83 ssibly due to the increase in protonation in polyatomic sputtering, and coronene was found to further

84 nderstanding of mode-selective reactivity in polyatomic systems.

85 collisional relaxation is prevalent in other polyatomic systems.

86 te dynamics to increasingly multidimensional polyatomic systems.

87 ers, ammonia clusters, and mixed dimers with polyatomic units are reviewed for completion and compari