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1 olet/visible (UV/vis) electronic absorption, multinuclear NMR, X-band electron paramagnetic resonance
2 R vibrational, UV/vis electronic absorption, multinuclear NMR, X-band EPR, and X-ray absorption spect
3 zed and characterized by elemental analysis, multinuclear NMR spectroscopy, X-ray crystallography, an
4 zed by X-ray crystallography (Zn and Cd) and multinuclear NMR spectroscopy.
5 tices confirmed by X-ray crystallography and multinuclear NMR for Ag(I).
6 were extensively analyzed by IR, EA DTA, and multinuclear NMR spectroscopy.
7 ned 3D zeolite counterpart, whereas FTIR and multinuclear NMR spectroscopies demonstrate synthesis of
8 nthesized and characterized by infrared, and multinuclear NMR spectra, and elemental analyses.
9 pounds were fully characterized using IR and multinuclear NMR spectroscopy, elemental analysis (EA),
10 pounds were fully characterized using IR and multinuclear NMR spectroscopy, elemental analysis, and d
11 pounds were fully characterized using IR and multinuclear NMR spectroscopy, elemental analysis, natur
12 of the protein in a eukaryotic cell line and multinuclear NMR spectroscopy.
13 d by X-ray diffraction, (57)Fe Mossbauer and multinuclear NMR spectroscopy, and combustion analysis.
14 erized (elemental analyses, FT-IR, Raman and multinuclear NMR spectroscopy, ESI+ mass spectrometry, c
15  crystallography, UV-visible, IR, Raman, and multinuclear NMR spectroscopies, as well as by density f
16 required to reproduce the observed X-ray and multinuclear NMR structures.
17 with IR spectroscopy, mass spectrometry, and multinuclear NMR spectroscopy confirm that the organic b
18 y elemental analysis, mass spectrometry, and multinuclear NMR spectroscopy.
19 ysis, high-resolution mass spectrometry, and multinuclear NMR spectroscopy.
20 n fully characterized by IR spectroscopy and multinuclear NMR spectroscopy as well as by single-cryst
21 ystal X-ray diffraction, IR spectroscopy and multinuclear NMR spectroscopy.
22  were intensively studied by vibrational and multinuclear NMR spectroscopy ((1)H, (13)C, (14)N), diff
23 by X-ray crystallography and vibrational and multinuclear NMR spectroscopy.
24 ction, UV-vis spectroscopy, voltammetry, and multinuclear NMR), and in silico studies (DFT, TD-DFT, a
25                                Described are multinuclear NMR experiments at very low temperatures ai
26 acterized structurally and as appropriate by multinuclear NMR, CW X-band EPR (for Ti(III)), and HFEPR
27  robust, permitting full characterization by multinuclear NMR spectroscopy and single-crystal X-ray d
28         All assemblies were characterized by multinuclear NMR ((1)H and (31)P), mass spectrometry (ES
29 or surface, have been fully characterized by multinuclear NMR ((31)P and (1)H) and electrospray ioniz
30 ), 2 = (Me-DuPHOS)(2)) were characterized by multinuclear NMR and CD spectroscopy in solution and by
31  rectangles have been fully characterized by multinuclear NMR and electrospray ionization mass spectr
32          Both ensembles are characterized by multinuclear NMR and electrospray ionization mass spectr
33      The two structures are characterized by multinuclear NMR and ESI-MS.
34    Pentafluoroferrocene was characterized by multinuclear NMR and IR spectroscopy, by cyclovoltammetr
35 , has now been prepared and characterized by multinuclear NMR and Raman spectroscopy.
36 uclear dihydrido Ni complex characterized by multinuclear NMR and single-crystal X-ray diffraction an
37              Compound 1 was characterized by multinuclear NMR and X-ray crystallography.
38     The compounds have been characterized by multinuclear NMR spectroscopy and electrospray ionizatio
39 .[H][OR] and 2.[H][NHR] are characterized by multinuclear NMR spectroscopy and X-ray crystallography,
40 bamate were synthesized and characterized by multinuclear NMR spectroscopy and X-ray crystallography.
41      All products have been characterized by multinuclear NMR spectroscopy and X-ray crystallography.
42 ollide NHC, which was fully characterized by multinuclear NMR spectroscopy as well as single-crystal
43 exes have been isolated and characterized by multinuclear NMR spectroscopy as well as X-ray diffracti
44 produced cations were fully characterized by multinuclear NMR spectroscopy at low temperature, and th
45           The compounds are characterized by multinuclear NMR spectroscopy, electrospray ionization m
46              Compound 3 was characterized by multinuclear NMR spectroscopy, mass spectrometry, single
47 mplexes of uranium and were characterized by multinuclear NMR spectroscopy, single crystal X-ray diff
48 spholium triflate salts are characterized by multinuclear NMR spectroscopy, X-ray analysis, as well a
49 omplexes were unambiguously characterized by multinuclear NMR spectroscopy.
50 % isolated yields and fully characterized by multinuclear NMR, 2D NMR, electrospray ionization time-o
51 l complexes have been fully characterized by multinuclear NMR, FT-IR, isotopic labeling, and, in most
52  and all of them were fully characterized by multinuclear NMR, FTIR spectroscopy, elemental analysis,
53 lated and spectroscopically characterized by multinuclear NMR, IR, and UV/vis spectroscopy, crystallo
54 charged macromolecules were characterized by multinuclear NMR, mass spectrometry, and physical means.
55   These gold compounds were characterized by multinuclear NMR, microanalysis, mass spectrometry, and
56 tuted derivatives have been characterized by multinuclear NMR.
57 tically prepared, its structure confirmed by multinuclear NMR and high resolution mass spectrometry,
58 re of the interactions has been confirmed by multinuclear NMR spectroscopy.
59 dented chiral environment as demonstrated by multinuclear NMR and single-crystal X-ray studies.
60 es 2-5 have been unambiguously determined by multinuclear NMR spectroscopy and crystallography.
61 sence of the nickel iminyl was determined by multinuclear NMR spectroscopy observed during catalysis.
62 coordinate silicon centers, as determined by multinuclear NMR spectroscopy, X-ray crystallography, an
63 ture of the UQ(1-51) dimer was determined by multinuclear NMR spectroscopy.
64 ecular E...O interactions was established by multinuclear NMR spectroscopy, single crystal X-ray anal
65 solution has been thoroughly investigated by multinuclear NMR spectroscopy.
66 ion, exclusive O-protonation was observed by multinuclear NMR spectroscopy.
67                The nature of 3 was probed by multinuclear NMR spectroscopy, single-crystal X-ray diff
68  the rate of ethane elimination reactions by multinuclear NMR spectroscopy provides evidence for a se
69                             Here, we show by multinuclear NMR spectroscopy that substitution of C for
70  which has been characterized in solution by multinuclear NMR.
71  Rap30 DNA-binding domain has been solved by multinuclear NMR spectroscopy.
72 nd behavior in solution have been studied by multinuclear NMR spectroscopy, which supports specific i
73 in in the Mb heme pocket has been studied by multinuclear NMR with an (15)N labeled zinc porphyrin de
74  formation of the structures is supported by multinuclear NMR, ESI FT-ICR mass spectrometry, and elem
75 erization of the supramolecular triangles by multinuclear NMR, elemental analysis, and electrospray m
76                 Solution-spectroscopic data (multinuclear NMR, IR) for 2a,b, and the solid-state stru
77 ent (X-ray diffraction, neutron diffraction, multinuclear NMR), computational methods (DFT, QTAIM, NC
78   Extensive mechanistic studies encompassing multinuclear NMR spectroscopy, deuterium labeling, rearr
79                                 An extensive multinuclear NMR study of natural abundance and (6)Li an
80 inding sites of Gluc(-) were identified from multinuclear NMR measurements.
81     The molecules are characterized by FTIR, multinuclear NMR, mass spectrometry, and Rutherford back
82 ies of these compounds were studied by FTIR, multinuclear NMR, mass spectrometry, Rutherford backscat
83 have been characterized using (31)P and (1)H multinuclear NMR spectroscopy and electrospray ionizatio
84 m resonances and their splitting patterns in multinuclear NMR spectra of 2H indicate that the chiral
85 actions and fully characterized by infrared, multinuclear NMR spectra, and elemental analysis.
86 the compounds were characterized through IR, multinuclear NMR spectroscopy, high-resolution mass spec
87                                      A joint multinuclear NMR spectroscopy and density functional the
88 complexes have been characterized by ESI-MS, multinuclear NMR, and DFT calculations.
89                            Multidimensional, multinuclear NMR has the potential to elucidate the mech
90                            Multidimensional, multinuclear NMR spectroscopy was used to determine the
91 rsenate to arsenite, using multidimensional, multinuclear NMR.
92 thod is presented for concurrently obtaining multinuclear NMR spectra using a single RF channel.
93 f the reactions was assessed with the aid of multinuclear NMR spectroscopy and X-ray crystallography.
94 all been characterized by a diverse array of multinuclear NMR spectroscopic experiments including (1)
95   Characterization involves a combination of multinuclear NMR spectroscopy, combustion analysis, DFT
96  NO(x) were investigated by a combination of multinuclear NMR techniques and DFT calculations, which
97 uilding blocks were investigated by means of multinuclear NMR spectroscopy and by fast atom bombardme
98                                 A variety of multinuclear NMR techniques, in combination with X-ray d
99 her with these control experiments, rigorous multinuclear NMR analysis, and quantum-chemical calculat
100                                     Solution multinuclear NMR experiments validate the boravinylidene
101 ePh, 5a; Ph2, 5b) using variable temperature multinuclear NMR spectroscopy (-80 to 20 degrees C).
102                             Low-temperature, multinuclear NMR studies provided quantitative informati
103                                          The multinuclear NMR data demonstrate the utility of this ce
104                                         This multinuclear NMR study demonstrates that diffraction alo
105 )][BPh(4)] (7) which was characterized using multinuclear NMR and high-resolution mass spectrometry.
106 The chemical structures were confirmed using multinuclear NMR spectroscopy ((1)H, (13)C, (19)F, and (
107  these reactions were studied in depth using multinuclear NMR experiments, monitoring the reactions i
108 their electronic structures elucidated using multinuclear NMR, EPR, electronic absorption spectroscop
109 hDHFR and hDHFR-NADPH was investigated using multinuclear NMR techniques.
110 oring of the tandem catalytic reaction using multinuclear NMR spectroscopy with syngas mixtures.
111 -ray diffraction (XRD) and in solution using multinuclear NMR methods (including DOSY, EXSY, and COSY
112      Their structures were characterized via multinuclear NMR and X-ray crystallography.
113 )Si = MeCl(2)Si) was fully characterized via multinuclear NMR spectroscopy and X-ray crystal structur
114 II) hydride compounds were characterized via multinuclear NMR spectroscopy, infrared spectroscopy, an
115 ranium complexes have been characterized via multinuclear NMR, vibrational, and electronic absorption
116 sis, all these complexes were elucidated via multinuclear NMR experiments and isotopic labelling stud
117 tity of [1](*+) is supported by EPR, UV-vis, multinuclear NMR ((1)H, (11)B), and X-ray photoelectron
118 ds, as well as (57)Fe Mossbauer, IR, UV/vis, multinuclear NMR, and dual-mode EPR spectroscopy.
119       Characterization was accomplished with multinuclear NMR and UV-vis spectroscopy, FAB mass spect
120       The assemblies were characterized with multinuclear NMR ((1)H and (31)P), mass spectrometry (ES
121  All three TBP cages were characterized with multinuclear NMR and electrospray ionization mass spectr
122  and building blocks were characterized with multinuclear NMR spectroscopy, electrospray ionization m

 
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