CO-DEPOSITION OF FULLERENES AND SULFUR FROM DILUTED SOLUTION.
Saved in:
| Title: | CO-DEPOSITION OF FULLERENES AND SULFUR FROM DILUTED SOLUTION. |
|---|---|
| Authors: | Takahashi, H., Matsubara, E., Shiro, M., Matsubara, S., Sato, N., Muramatsu, A., Tohji, K. |
| Source: | Fullerenes, Nanotubes & Carbon Nanostructures. Aug2002, Vol. 10 Issue 3, p217. 10p. |
| Subjects: | Fullerenes, Sulfur |
| Abstract: | A new method to synthesize fullerene and sulfur compounds has been developed. Using this method, C60S16 and C70S16 compounds were grown from dilute fullerene and sulfur toluene solution. Their atomic structures were analyzed by x-ray diffraction with the single crystal. The C60S16 crystal is C-centered monoclinic structure of a=2.0874 nm, b=2.1139 nm, c=1.05690 nm and β=111.93?, and the C70S16 has a primitive monoclinic, P21/c, with lattice parameters of a=1.5271 nm, b=1.49971 nm, c=2.18024 nm and β=109.791?. In this compound, the structure of fullerenes is maintained and sulfur atoms form S8 rings placed around the fullerenes. [ABSTRACT FROM AUTHOR] |
| Copyright of Fullerenes, Nanotubes & Carbon Nanostructures is the property of Taylor & Francis Ltd and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.) | |
| Database: | Engineering Source |
| FullText | Text: Availability: 0 |
|---|---|
| Header | DbId: egs DbLabel: Engineering Source An: 7415587 AccessLevel: 6 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
| IllustrationInfo | |
| Items | – Name: Title Label: Title Group: Ti Data: CO-DEPOSITION OF FULLERENES AND SULFUR FROM DILUTED SOLUTION. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Takahashi%2C+H%2E%22">Takahashi, H.</searchLink><br /><searchLink fieldCode="AR" term="%22Matsubara%2C+E%2E%22">Matsubara, E.</searchLink><br /><searchLink fieldCode="AR" term="%22Shiro%2C+M%2E%22">Shiro, M.</searchLink><br /><searchLink fieldCode="AR" term="%22Matsubara%2C+S%2E%22">Matsubara, S.</searchLink><br /><searchLink fieldCode="AR" term="%22Sato%2C+N%2E%22">Sato, N.</searchLink><br /><searchLink fieldCode="AR" term="%22Muramatsu%2C+A%2E%22">Muramatsu, A.</searchLink><br /><searchLink fieldCode="AR" term="%22Tohji%2C+K%2E%22">Tohji, K.</searchLink> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22Fullerenes%2C+Nanotubes+%26+Carbon+Nanostructures%22">Fullerenes, Nanotubes & Carbon Nanostructures</searchLink>. Aug2002, Vol. 10 Issue 3, p217. 10p. – Name: Subject Label: Subjects Group: Su Data: <searchLink fieldCode="DE" term="%22Fullerenes%22">Fullerenes</searchLink><br /><searchLink fieldCode="DE" term="%22Sulfur%22">Sulfur</searchLink> – Name: Abstract Label: Abstract Group: Ab Data: A new method to synthesize fullerene and sulfur compounds has been developed. Using this method, C60S16 and C70S16 compounds were grown from dilute fullerene and sulfur toluene solution. Their atomic structures were analyzed by x-ray diffraction with the single crystal. The C60S16 crystal is C-centered monoclinic structure of a=2.0874 nm, b=2.1139 nm, c=1.05690 nm and β=111.93?, and the C70S16 has a primitive monoclinic, P21/c, with lattice parameters of a=1.5271 nm, b=1.49971 nm, c=2.18024 nm and β=109.791?. In this compound, the structure of fullerenes is maintained and sulfur atoms form S8 rings placed around the fullerenes. [ABSTRACT FROM AUTHOR] – Name: AbstractSuppliedCopyright Label: Group: Ab Data: <i>Copyright of Fullerenes, Nanotubes & Carbon Nanostructures is the property of Taylor & Francis Ltd and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract.</i> (Copyright applies to all Abstracts.) |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=egs&AN=7415587 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1081/FST-120014736 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 10 StartPage: 217 Subjects: – SubjectFull: Fullerenes Type: general – SubjectFull: Sulfur Type: general Titles: – TitleFull: CO-DEPOSITION OF FULLERENES AND SULFUR FROM DILUTED SOLUTION. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Takahashi, H. – PersonEntity: Name: NameFull: Matsubara, E. – PersonEntity: Name: NameFull: Shiro, M. – PersonEntity: Name: NameFull: Matsubara, S. – PersonEntity: Name: NameFull: Sato, N. – PersonEntity: Name: NameFull: Muramatsu, A. – PersonEntity: Name: NameFull: Tohji, K. IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 08 Text: Aug2002 Type: published Y: 2002 Identifiers: – Type: issn-print Value: 1536383X Numbering: – Type: volume Value: 10 – Type: issue Value: 3 Titles: – TitleFull: Fullerenes, Nanotubes & Carbon Nanostructures Type: main |
| ResultId | 1 |