Sulfur, not too far behind O, N, and C: SH...pi hydrogen bond.
about
Energy decomposition analysis of cation-π, metal ion-lone pair, hydrogen bonded, charge-assisted hydrogen bonded, and π-π interactions.Physics-based scoring of protein-ligand interactions: explicit polarizability, quantum mechanics and free energies.The role of Cysteine 6.47 in class A GPCRsMolecular-level understanding of ground- and excited-state O-H...O hydrogen bonding involving the tyrosine side chain: a combined high-resolution laser spectroscopy and quantum chemistry study.Intra-residue interactions in proteins: interplay between serine or cysteine side chains and backbone conformations, revealed by laser spectroscopy of isolated model peptides.Functionally important aromatic-aromatic and sulfur-π interactions in the D2 dopamine receptor.Experimental quantification of electrostatics in X-H···π hydrogen bondsAromatic rings in chemical and biological recognition: energetics and structures.Synthesis of a large functional cage compound based on four Ga-Ga single bonds and its application as an oligoacceptor: on the way to bio-organogallium hybrid molecules.Microwave, infrared-microwave double resonance, and theoretical studies of C2H4···H2S complex.Interpretation of Spectroscopic Markers of Hydrogen Bonds.Nature and Strength of the Inner-Core H⋅⋅⋅H Interactions in Porphyrinoids.Insights into Thiol-Aromatic Interactions: A Stereoelectronic Basis for S-H/π Interactions.SH···N and SH···P blue-shifting H-bonds and N···P interactions in complexes pairing HSN with amines and phosphines.Isomer selective IR-UV depletion spectroscopy of 4-fluorotoluene-NH3: evidence for π-proton-acceptor and linear hydrogen-bonded complexes.Excited-state N-H···S hydrogen bond between indole and dimethyl sulfide: time-dependent density functional theory study.Comparison of P···D (D = P,N) with other noncovalent bonds in molecular aggregates.On the properties of Se⋯N interaction: the analysis of substituent effects by energy decomposition and orbital interaction.Structures of protonated hydrogen sulfide clusters, H+(H2S)n, highlighting the nature of sulfur-centered intermolecular interactions.Structural investigations on a linear isolated depsipeptide: the importance of dispersion interactions.Unexpected solvent effects on the UV/Vis absorption spectra of o-cresol in toluene and benzene: in contrast with non-aromatic solvents.
P2860
Q30009250-0F1ECA81-11B0-4882-82CD-7F89C3481BA5Q33893098-C21D4426-8216-40C9-9753-22772EA22996Q34623053-92230989-6A35-427B-B833-2C498E845BF7Q35033951-5E5E7DCF-CB98-42EB-818B-5C90A46BEF16Q35497835-B4A733C8-7627-433A-B6EA-D66CDF6B220BQ36288129-E6154400-E394-4749-90F5-3D8AE7D95D60Q36438738-CB386DEC-FB0E-4CB3-A19F-DFDF6444BD23Q37871537-A8DF2598-09DE-4EB3-8268-63E0C74F10A3Q45823490-C6DCDDBD-F578-4B4A-B44E-A9FFCD1F44A6Q46299504-D3B423F6-F90B-44F2-BA1D-3AB0707AA835Q46569227-3DAFF234-FD9E-40BD-8CE8-356F4CB6A395Q48052348-6772FB3C-C003-4B3E-BE3F-F88F42BB3C8CQ48358876-1242F56A-4786-4CA4-81B2-3FB3E5416B9EQ50284009-56294854-B547-40D0-9BF1-BE92CEB0CEB0Q50436426-91A61DCA-F16A-483F-84FA-3525E012DCA1Q50528811-CD915EEC-6AE8-4D42-9837-D6779238B53EQ52730805-E13987A2-AC8A-42A2-88FD-A98F8DD821B9Q53324398-429B82BD-BE29-412D-B81F-FEAD1A324DB3Q53613796-F6332448-D992-4238-9832-8424CAE1DE51Q54091895-210BAD6D-4F79-4D96-9A43-F55E6B6B3CA8Q55196286-E33F28EF-AFB2-415B-889C-58E6E288244B
P2860
Sulfur, not too far behind O, N, and C: SH...pi hydrogen bond.
description
2009 nî lūn-bûn
@nan
2009 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
Sulfur, not too far behind O, N, and C: SH...pi hydrogen bond.
@ast
Sulfur, not too far behind O, N, and C: SH...pi hydrogen bond.
@en
Sulfur, not too far behind O, N, and C: SH...pi hydrogen bond.
@nl
type
label
Sulfur, not too far behind O, N, and C: SH...pi hydrogen bond.
@ast
Sulfur, not too far behind O, N, and C: SH...pi hydrogen bond.
@en
Sulfur, not too far behind O, N, and C: SH...pi hydrogen bond.
@nl
prefLabel
Sulfur, not too far behind O, N, and C: SH...pi hydrogen bond.
@ast
Sulfur, not too far behind O, N, and C: SH...pi hydrogen bond.
@en
Sulfur, not too far behind O, N, and C: SH...pi hydrogen bond.
@nl
P356
P1476
Sulfur, not too far behind O, N, and C: SH...pi hydrogen bond.
@en
P2093
Sanjay Wategaonkar
P304
12774-12782
P356
10.1021/JP907747W
P407
P577
2009-11-01T00:00:00Z