Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Nikola, Bedeković"'
Publikováno v:
Crystal Growth & Design. 22:7508-7517
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::773b4ed4e1863df11fffab75375b854e
https://doi.org/10.1021/acs.cgd.2c01055
https://doi.org/10.1021/acs.cgd.2c01055
Publikováno v:
Crystals, Vol 11, Iss 6, p 699 (2021)
In order to study the effect of halogen bond on tautomerism in β-diketones in the solid-state, we have prepared a series of cocrystals derived from an asymmetric β-diketone, benzoyl-4-pyridoylmethane (b4pm), as halogen bond acceptor and perfluorina
Externí odkaz:
https://doaj.org/article/802901ac8bea4a639680125d7f3ac9eb
Publikováno v:
Crystals, Vol 11, Iss 5, p 529 (2021)
In order to study the proclivity of primary amine groups to act as halogen bond acceptors, three aromatic diamines (p-phenylenediamine (pphda), benzidine (bnzd) and o-tolidine (otol)) were cocrystallised with three perfluorinated iodobenzenes (1,4-te
Externí odkaz:
https://doaj.org/article/305e51bfc4cf45808e0e55b11cf06f88
Publikováno v:
Crystal Growth & Design. 22:3981-3989
Six novel halogen-bonded cocrystals of 1, 3, 5- triiodo-2, 4, 6-trifluorobenzene with three structural isomers of benzoylpyridine have been synthesized mechanochemically and by crystallization from solution, five of which were structurally characteri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9d4438e7e67575231d7749ccd8bfbbfa
https://doi.org/10.1021/acs.cgd.2c00382
https://doi.org/10.1021/acs.cgd.2c00382
Publikováno v:
Crystal Growth & Design. 22:987-992
Seven cocrystals of pyridone and perfluorinated halocarbons have been prepared. In all cases pairs of pyridone molecules are connected into dimers by two N–H···O hydrogen bonds, forming the characteristic pyridone homosynthon of R22(8) topology.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3e08ffa3299e37311b783c8ef744a1f5
https://doi.org/10.1021/acs.cgd.1c01424
https://doi.org/10.1021/acs.cgd.1c01424
In order to study the potential of Keggin type polyoxometalate anions to act as halogen bond acceptors we have prepared a series of 10 halogen- bonded compounds starting from phosphomolybdic and phosphotungstic acid and halogenopyridinium cations as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b661bfb467e78af35a44e6916547ea83
https://www.bib.irb.hr/1270185
https://www.bib.irb.hr/1270185
Publikováno v:
Crystal growthdesign. 22(9)
In this study, we investigate the halogen bond acceptor potential of oxygen and nitrogen atoms of morpholine and piperazine fragments when they are peripherally located on
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8b4ae8f9838c7fcfe1017b7036f6bf4d
https://pubmed.ncbi.nlm.nih.gov/36097548
https://pubmed.ncbi.nlm.nih.gov/36097548
Six N-(4-halogenobenzyl)-3-halogenopyridinium cations were prepared by reacting meta-halogenopyridines (Cl, Br, and I) with (4-halogenobenzyl) bromides (Br and I) and were isolated as bromide salts, which were further used to obtain iodides and chlor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5a529e5e60d94196b904588ef5d35fed
https://doi.org/10.1021/acs.cgd.1c01285
https://doi.org/10.1021/acs.cgd.1c01285
To investigate influences on the topicity of perfluorinated halobenzenes as halogen bond (XB) donors in the solid state, we have conducted a database survey and prepared 18 novel cocrystals of potentially ditopic (13ditfb, 14ditfb) and tritopic (135t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::635c21b0627db8d40b8a9c935a730c32
https://doi.org/10.1021/acs.cgd.2c00077
https://doi.org/10.1021/acs.cgd.2c00077
In this study, we investigate the halogen bond acceptor potential of oxygen and nitrogen atoms of morpholine and piperazine fragments when they are peripherally located on N, O, O or N, N, O acceptor molecules. We synthesized four acceptor molecules
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::44cbc9e93b563c4ea9b7a0543955fcf7
https://doi.org/10.1021/acs.cgd.2c00665
https://doi.org/10.1021/acs.cgd.2c00665