2009
DOI: 10.1021/ja901854t
|View full text |Cite
|
Sign up to set email alerts
|

Alkyl Radicals as Hydrogen Bond Acceptors: Computational Evidence

Abstract: Spectroscopic, energetic and structural information obtained by DFT and G3-type computational studies demonstrates that charged proton donors can form moderately strong hydrogen bonds to simple alkyl radicals. The presence of these bonds stabilizes the adducts and modifies their structure, and gives rise to pronounced shifts of IR stretching frequencies and to increased absorption intensities. The hydrogen bond acceptor properties of alkyl radicals equal those of many conventional acceptors, e.g., the bond len… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
4
1

Citation Types

1
45
0
1

Year Published

2009
2009
2023
2023

Publication Types

Select...
9

Relationship

0
9

Authors

Journals

citations
Cited by 50 publications
(47 citation statements)
references
References 155 publications
1
45
0
1
Order By: Relevance
“…There is a relationship between wavelength, absorbance and ion concentration, for most ions and ion adducts (including NaCl [215,216], ClxOy [217][218][219][220], Cl2 − [220], ClxOyHz [218], OxH [221][222][223][224][225], Ox n− [225], FeOOH [93,226], Fe(OH)x [226], n-Fe 0 [227]). Absorbance increases (or decreases), at specific wavelengths, as the ion concentration increases [228].…”
Section: E1 Assessment Of Product Water Salinity Using Uv-visible Spmentioning
confidence: 99%
“…There is a relationship between wavelength, absorbance and ion concentration, for most ions and ion adducts (including NaCl [215,216], ClxOy [217][218][219][220], Cl2 − [220], ClxOyHz [218], OxH [221][222][223][224][225], Ox n− [225], FeOOH [93,226], Fe(OH)x [226], n-Fe 0 [227]). Absorbance increases (or decreases), at specific wavelengths, as the ion concentration increases [228].…”
Section: E1 Assessment Of Product Water Salinity Using Uv-visible Spmentioning
confidence: 99%
“…Unlike the initial days of hydrogen bonding when lone pairs of N, O or F were thought to be the only hydrogen bond acceptors, 10 it has now been recognised that any electron-rich region in a molecule, such as a lone pair, π pair, unpaired electron and sigma electrons, can be hydrogen bond acceptors. [11][12][13][14] The recent IUPAC report and recommendation on hydro gen bond have recognised the diverse nature of hydrogen bond donors and acceptors. 13,14 Unlike methane, hydrogen bonding by higher alkanes has not received much attention.…”
Section: Introductionmentioning
confidence: 99%
“…10 o modelo clássico da ligação de hidrogênio (X-Y -δ •••H +δ -Z) também coexistir em uma interação do tipo van der Waals?" De acordo com a proposta de Bian 64 utilizada para medir a força da ligação de hidrogê-nio, e nos argumentos de Hammerum 65 sobre a utilização de radicais alquila como receptores de prótons, é incontestável que a natureza das espécies X-Y e H-Z promova não somente a formação da supermolécula, mas que também seja um guia para investigar a intensidade de interação. No que diz respeito à estabilidade intermolecular, a interpretação das energias potenciais de atração e repulsão existentes entre X-Y e H-Z inegavelmente conduz a um discernimento mais coerente sobre a interação reinante, conforme ilustra a Figura 1.…”
Section: Introductionunclassified