Hydrophobic hydration of the hydrocarbon adamantane in amorphous ice
Hydrophobic molecules are by definition difficult to hydrate. Previous studies in the area of hydrophobic hydration have therefore often relied on using amphiphilic molecules where the hydrophilic part of a molecule enabled the solubility in liquid water. Here, we show that the hydrophobic adamantan...
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description | Hydrophobic molecules are by definition difficult to hydrate. Previous studies in the area of hydrophobic hydration have therefore often relied on using amphiphilic molecules where the hydrophilic part of a molecule enabled the solubility in liquid water. Here, we show that the hydrophobic adamantane (C
10
H
16
) molecule can be fully hydrated through vapour codeposition with water onto a cryogenic substrate at 80 K resulting in the matrix isolation of adamantane in amorphous ice. Using neutron diffraction in combination with the isotopic substitution method and the empirical potential structure refinement technique, we find that the first hydration shell of adamantane is well structured consisting of a hydrogen-bonded cage of 28 water molecules that is also found in cubic structure II clathrate hydrates. The four hexagonal faces of the 5
12
6
4
cage are situated above the four methine (CH) groups of adamantane whereas the methylene (CH
2
) groups are positioned below the edges of two adjoining pentagonal faces. The oxygen atoms of the 28 water molecules can be categorised on the basis of symmetry equivalences as twelve A, twelve B and four C oxygens. The water molecules of the first hydration shell display orientations consistent with those expected for a clathrate-hydrate-type cage, but also unfavourable ones with respect to the hydrogen bonding between the water molecules. Annealing the samples at 140 K, which is just below the crystallisation temperature of the matrix, removes the unfavourable orientations and leads to a slight increase in the structural order of the first hydration shell. The very closest water molecules display a tendency for their dipole moments to point towards the adamantane which is attributed to steric effects. Other than this, no significant polarisation effects are observed which is consistent with weak interactions between adamantane and the amorphous ice matrix. FT-IR spectroscopy shows that the incorporation of adamantane into amorphous ice leads to a weakening of the hydrogen bonds. In summary, the matrix-isolation of the highly symmetric adamantane in amorphous ice provides an interesting test case for hydrophobic hydration. Studying the structure and spectroscopic properties of water at the interface with hydrophobic hydrocarbons is also relevant for astrophysical environments, such as comets or the interstellar medium, where amorphous ice and hydrocarbons have been shown to coexist in large quantities.
The hydrophobic a |
doi_str_mv | 10.1039/d3fd00102d |
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10
H
16
) molecule can be fully hydrated through vapour codeposition with water onto a cryogenic substrate at 80 K resulting in the matrix isolation of adamantane in amorphous ice. Using neutron diffraction in combination with the isotopic substitution method and the empirical potential structure refinement technique, we find that the first hydration shell of adamantane is well structured consisting of a hydrogen-bonded cage of 28 water molecules that is also found in cubic structure II clathrate hydrates. The four hexagonal faces of the 5
12
6
4
cage are situated above the four methine (CH) groups of adamantane whereas the methylene (CH
2
) groups are positioned below the edges of two adjoining pentagonal faces. The oxygen atoms of the 28 water molecules can be categorised on the basis of symmetry equivalences as twelve A, twelve B and four C oxygens. The water molecules of the first hydration shell display orientations consistent with those expected for a clathrate-hydrate-type cage, but also unfavourable ones with respect to the hydrogen bonding between the water molecules. Annealing the samples at 140 K, which is just below the crystallisation temperature of the matrix, removes the unfavourable orientations and leads to a slight increase in the structural order of the first hydration shell. The very closest water molecules display a tendency for their dipole moments to point towards the adamantane which is attributed to steric effects. Other than this, no significant polarisation effects are observed which is consistent with weak interactions between adamantane and the amorphous ice matrix. FT-IR spectroscopy shows that the incorporation of adamantane into amorphous ice leads to a weakening of the hydrogen bonds. In summary, the matrix-isolation of the highly symmetric adamantane in amorphous ice provides an interesting test case for hydrophobic hydration. Studying the structure and spectroscopic properties of water at the interface with hydrophobic hydrocarbons is also relevant for astrophysical environments, such as comets or the interstellar medium, where amorphous ice and hydrocarbons have been shown to coexist in large quantities.
The hydrophobic adamantane molecule is fully hydrated through vapour codeposition with water onto a cryogenic substrate and the structure of the first hydration shell is studied with neutron diffraction.</description><identifier>ISSN: 1359-6640</identifier><identifier>EISSN: 1364-5498</identifier><identifier>DOI: 10.1039/d3fd00102d</identifier><identifier>PMID: 37794776</identifier><language>eng</language><publisher>England: Royal Society of Chemistry</publisher><subject>Bonding strength ; Cages ; Chemistry ; Codeposition ; Comets ; Crystallization ; Dipole moments ; Equivalence ; Gas hydrates ; Hydration ; Hydrocarbons ; Hydrogen bonding ; Hydrogen bonds ; Hydrophobicity ; Infrared spectroscopy ; Interstellar matter ; Mathematical analysis ; Matrices (mathematics) ; Neutron diffraction ; Neutrons ; Oxygen atoms ; Steric effects ; Substrates ; Symmetry ; Water ; Water chemistry</subject><ispartof>Faraday discussions, 2024-02, Vol.249, p.69-83</ispartof><rights>Copyright Royal Society of Chemistry 2024</rights><rights>This journal is © The Royal Society of Chemistry 2024 The Royal Society of Chemistry</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c388t-bd669be7bccdc9f67cc7ca62f29051bfd3e3e0c794edd5467f1340bdf9f110fa3</cites><orcidid>0000-0002-0714-7342 ; 0000-0003-0095-5731 ; 0000-0002-2768-0013</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37794776$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Talewar, Sukhpreet K</creatorcontrib><creatorcontrib>Pardo, Luis Carlos</creatorcontrib><creatorcontrib>Headen, Thomas F</creatorcontrib><creatorcontrib>Halukeerthi, Siriney O</creatorcontrib><creatorcontrib>Chikani, Bharvi</creatorcontrib><creatorcontrib>Rosu-Finsen, Alexander</creatorcontrib><creatorcontrib>Salzmann, Christoph G</creatorcontrib><title>Hydrophobic hydration of the hydrocarbon adamantane in amorphous ice</title><title>Faraday discussions</title><addtitle>Faraday Discuss</addtitle><description>Hydrophobic molecules are by definition difficult to hydrate. Previous studies in the area of hydrophobic hydration have therefore often relied on using amphiphilic molecules where the hydrophilic part of a molecule enabled the solubility in liquid water. Here, we show that the hydrophobic adamantane (C
10
H
16
) molecule can be fully hydrated through vapour codeposition with water onto a cryogenic substrate at 80 K resulting in the matrix isolation of adamantane in amorphous ice. Using neutron diffraction in combination with the isotopic substitution method and the empirical potential structure refinement technique, we find that the first hydration shell of adamantane is well structured consisting of a hydrogen-bonded cage of 28 water molecules that is also found in cubic structure II clathrate hydrates. The four hexagonal faces of the 5
12
6
4
cage are situated above the four methine (CH) groups of adamantane whereas the methylene (CH
2
) groups are positioned below the edges of two adjoining pentagonal faces. The oxygen atoms of the 28 water molecules can be categorised on the basis of symmetry equivalences as twelve A, twelve B and four C oxygens. The water molecules of the first hydration shell display orientations consistent with those expected for a clathrate-hydrate-type cage, but also unfavourable ones with respect to the hydrogen bonding between the water molecules. Annealing the samples at 140 K, which is just below the crystallisation temperature of the matrix, removes the unfavourable orientations and leads to a slight increase in the structural order of the first hydration shell. The very closest water molecules display a tendency for their dipole moments to point towards the adamantane which is attributed to steric effects. Other than this, no significant polarisation effects are observed which is consistent with weak interactions between adamantane and the amorphous ice matrix. FT-IR spectroscopy shows that the incorporation of adamantane into amorphous ice leads to a weakening of the hydrogen bonds. In summary, the matrix-isolation of the highly symmetric adamantane in amorphous ice provides an interesting test case for hydrophobic hydration. Studying the structure and spectroscopic properties of water at the interface with hydrophobic hydrocarbons is also relevant for astrophysical environments, such as comets or the interstellar medium, where amorphous ice and hydrocarbons have been shown to coexist in large quantities.
The hydrophobic adamantane molecule is fully hydrated through vapour codeposition with water onto a cryogenic substrate and the structure of the first hydration shell is studied with neutron diffraction.</description><subject>Bonding strength</subject><subject>Cages</subject><subject>Chemistry</subject><subject>Codeposition</subject><subject>Comets</subject><subject>Crystallization</subject><subject>Dipole moments</subject><subject>Equivalence</subject><subject>Gas hydrates</subject><subject>Hydration</subject><subject>Hydrocarbons</subject><subject>Hydrogen bonding</subject><subject>Hydrogen bonds</subject><subject>Hydrophobicity</subject><subject>Infrared spectroscopy</subject><subject>Interstellar matter</subject><subject>Mathematical analysis</subject><subject>Matrices (mathematics)</subject><subject>Neutron diffraction</subject><subject>Neutrons</subject><subject>Oxygen atoms</subject><subject>Steric effects</subject><subject>Substrates</subject><subject>Symmetry</subject><subject>Water</subject><subject>Water chemistry</subject><issn>1359-6640</issn><issn>1364-5498</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNpdkUtLAzEUhYMotlY37pUBNyKM5jGTTFYirbVCwY2uQyYPO6UzqcmM0H9v-rA-Vrm598vhnhwAzhG8RZDwO02shhBBrA9AHxGapXnGi8N1nfOU0gz2wEkIcwghjdNj0COM8Ywx2gejyUp7t5y5slLJLNayrVyTOJu0M7NpOCV9GVtSy1o2rWxMUsVb7Xx81YWkUuYUHFm5COZsdw7A2_jxdThJpy9Pz8OHaapIUbRpqSnlpWGlUlpxS5lSTEmKLeYwR6XVxBADVVzNaJ1nlFlEMlhqyy1C0EoyAPdb3WVX1kYr07ReLsTSV7X0K-FkJf5Ommom3t2nQLDI8vhDUeF6p-DdR2dCK-oqKLNYRFvRjMAFIzhHGaIRvfqHzl3nm-hPYI4xoQzhteDNllLeheCN3W-DoFinI0ZkPNqkM4rw5e_99-h3HBG42AI-qP30J17yBUa8lZw</recordid><startdate>20240206</startdate><enddate>20240206</enddate><creator>Talewar, Sukhpreet K</creator><creator>Pardo, Luis Carlos</creator><creator>Headen, Thomas F</creator><creator>Halukeerthi, Siriney O</creator><creator>Chikani, Bharvi</creator><creator>Rosu-Finsen, Alexander</creator><creator>Salzmann, Christoph G</creator><general>Royal Society of Chemistry</general><general>The Royal Society of Chemistry</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-0714-7342</orcidid><orcidid>https://orcid.org/0000-0003-0095-5731</orcidid><orcidid>https://orcid.org/0000-0002-2768-0013</orcidid></search><sort><creationdate>20240206</creationdate><title>Hydrophobic hydration of the hydrocarbon adamantane in amorphous ice</title><author>Talewar, Sukhpreet K ; Pardo, Luis Carlos ; Headen, Thomas F ; Halukeerthi, Siriney O ; Chikani, Bharvi ; Rosu-Finsen, Alexander ; Salzmann, Christoph G</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c388t-bd669be7bccdc9f67cc7ca62f29051bfd3e3e0c794edd5467f1340bdf9f110fa3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Bonding strength</topic><topic>Cages</topic><topic>Chemistry</topic><topic>Codeposition</topic><topic>Comets</topic><topic>Crystallization</topic><topic>Dipole moments</topic><topic>Equivalence</topic><topic>Gas hydrates</topic><topic>Hydration</topic><topic>Hydrocarbons</topic><topic>Hydrogen bonding</topic><topic>Hydrogen bonds</topic><topic>Hydrophobicity</topic><topic>Infrared spectroscopy</topic><topic>Interstellar matter</topic><topic>Mathematical analysis</topic><topic>Matrices (mathematics)</topic><topic>Neutron diffraction</topic><topic>Neutrons</topic><topic>Oxygen atoms</topic><topic>Steric effects</topic><topic>Substrates</topic><topic>Symmetry</topic><topic>Water</topic><topic>Water chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Talewar, Sukhpreet K</creatorcontrib><creatorcontrib>Pardo, Luis Carlos</creatorcontrib><creatorcontrib>Headen, Thomas F</creatorcontrib><creatorcontrib>Halukeerthi, Siriney O</creatorcontrib><creatorcontrib>Chikani, Bharvi</creatorcontrib><creatorcontrib>Rosu-Finsen, Alexander</creatorcontrib><creatorcontrib>Salzmann, Christoph G</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Faraday discussions</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Talewar, Sukhpreet K</au><au>Pardo, Luis Carlos</au><au>Headen, Thomas F</au><au>Halukeerthi, Siriney O</au><au>Chikani, Bharvi</au><au>Rosu-Finsen, Alexander</au><au>Salzmann, Christoph G</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Hydrophobic hydration of the hydrocarbon adamantane in amorphous ice</atitle><jtitle>Faraday discussions</jtitle><addtitle>Faraday Discuss</addtitle><date>2024-02-06</date><risdate>2024</risdate><volume>249</volume><spage>69</spage><epage>83</epage><pages>69-83</pages><issn>1359-6640</issn><eissn>1364-5498</eissn><abstract>Hydrophobic molecules are by definition difficult to hydrate. Previous studies in the area of hydrophobic hydration have therefore often relied on using amphiphilic molecules where the hydrophilic part of a molecule enabled the solubility in liquid water. Here, we show that the hydrophobic adamantane (C
10
H
16
) molecule can be fully hydrated through vapour codeposition with water onto a cryogenic substrate at 80 K resulting in the matrix isolation of adamantane in amorphous ice. Using neutron diffraction in combination with the isotopic substitution method and the empirical potential structure refinement technique, we find that the first hydration shell of adamantane is well structured consisting of a hydrogen-bonded cage of 28 water molecules that is also found in cubic structure II clathrate hydrates. The four hexagonal faces of the 5
12
6
4
cage are situated above the four methine (CH) groups of adamantane whereas the methylene (CH
2
) groups are positioned below the edges of two adjoining pentagonal faces. The oxygen atoms of the 28 water molecules can be categorised on the basis of symmetry equivalences as twelve A, twelve B and four C oxygens. The water molecules of the first hydration shell display orientations consistent with those expected for a clathrate-hydrate-type cage, but also unfavourable ones with respect to the hydrogen bonding between the water molecules. Annealing the samples at 140 K, which is just below the crystallisation temperature of the matrix, removes the unfavourable orientations and leads to a slight increase in the structural order of the first hydration shell. The very closest water molecules display a tendency for their dipole moments to point towards the adamantane which is attributed to steric effects. Other than this, no significant polarisation effects are observed which is consistent with weak interactions between adamantane and the amorphous ice matrix. FT-IR spectroscopy shows that the incorporation of adamantane into amorphous ice leads to a weakening of the hydrogen bonds. In summary, the matrix-isolation of the highly symmetric adamantane in amorphous ice provides an interesting test case for hydrophobic hydration. Studying the structure and spectroscopic properties of water at the interface with hydrophobic hydrocarbons is also relevant for astrophysical environments, such as comets or the interstellar medium, where amorphous ice and hydrocarbons have been shown to coexist in large quantities.
The hydrophobic adamantane molecule is fully hydrated through vapour codeposition with water onto a cryogenic substrate and the structure of the first hydration shell is studied with neutron diffraction.</abstract><cop>England</cop><pub>Royal Society of Chemistry</pub><pmid>37794776</pmid><doi>10.1039/d3fd00102d</doi><tpages>15</tpages><orcidid>https://orcid.org/0000-0002-0714-7342</orcidid><orcidid>https://orcid.org/0000-0003-0095-5731</orcidid><orcidid>https://orcid.org/0000-0002-2768-0013</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Bonding strength Cages Chemistry Codeposition Comets Crystallization Dipole moments Equivalence Gas hydrates Hydration Hydrocarbons Hydrogen bonding Hydrogen bonds Hydrophobicity Infrared spectroscopy Interstellar matter Mathematical analysis Matrices (mathematics) Neutron diffraction Neutrons Oxygen atoms Steric effects Substrates Symmetry Water Water chemistry |
title | Hydrophobic hydration of the hydrocarbon adamantane in amorphous ice |
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