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Literature DB >> 12207502

Nanotube formation favored by chalcogen-chalcogen interactions.

Daniel B Werz¹, Rolf Gleiter, Frank Rominger.

Abstract

Close contacts between sulfur, selenium, and tellurium centers are used to construct nanotubes in the solid state which are able to host other molecules.

Entities: Chemical

Year: 2002 PMID： 12207502 DOI： 10.1021/ja027146d

Source DB: PubMed Journal: J Am Chem Soc ISSN： 0002-7863 Impact factor: 15.419

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Cited

13 in total

1. Chalcogen-bonded complexes. Selenium-bound adducts of NH3, H2O, PH3, and H2S with OCSe, SCSe, and CSe2.

Authors: Ponnadurai Ramasami; Thomas A Ford
Journal: J Mol Model Date: 2015-02-03 Impact factor: 1.810

2. Dual functions of Lewis acid and base of Se in F2C=Se and their interplay in F 2CSe•••NH 3•••HX.

Authors: Xin Guo; Qingzhong Li
Journal: J Mol Model Date: 2015-05-28 Impact factor: 1.810

3. Chalcogen- and halogen-bonds involving SX2 (X = F, Cl, and Br) with formaldehyde.

Authors: Lixin Mo; Yanli Zeng; Xiaoyan Li; Xueying Zhang; Lingpeng Meng
Journal: J Mol Model Date: 2016-06-24 Impact factor: 1.810

4. Substituent effects on the properties of the hemi-bonded complexes (XH2P···NH2Y)(+) (X, Y=H, F, Cl, Br, NH2, CH3, OH).

Authors: Li Fei Ji; An Yong Li; Zhuo Zhe Li; Zhi Xing Ge
Journal: J Mol Model Date: 2015-12-07 Impact factor: 1.810

5. Carbon-Halogen Bond Activation by Selenium-Based Chalcogen Bonding.

Authors: Patrick Wonner; Lukas Vogel; Maximilian Düser; Luís Gomes; Florian Kniep; Bert Mallick; Daniel B Werz; Stefan M Huber
Journal: Angew Chem Int Ed Engl Date: 2017-07-06 Impact factor: 15.336

6. Catalysis with chalcogen bonds: neutral benzodiselenazole scaffolds with high-precision selenium donors of variable strength.

Authors: Sebastian Benz; Jiri Mareda; Céline Besnard; Naomi Sakai; Stefan Matile
Journal: Chem Sci Date: 2017-10-16 Impact factor: 9.825

Nanotube formation favored by chalcogen-chalcogen interactions.

1. Chalcogen-bonded complexes. Selenium-bound adducts of NH3, H2O, PH3, and H2S with OCSe, SCSe, and CSe2.

2. Dual functions of Lewis acid and base of Se in F2C=Se and their interplay in F 2CSe•••NH 3•••HX.

3. Chalcogen- and halogen-bonds involving SX2 (X = F, Cl, and Br) with formaldehyde.

4. Substituent effects on the properties of the hemi-bonded complexes (XH2P···NH2Y)(+) (X, Y=H, F, Cl, Br, NH2, CH3, OH).

5. Carbon-Halogen Bond Activation by Selenium-Based Chalcogen Bonding.

6. Catalysis with chalcogen bonds: neutral benzodiselenazole scaffolds with high-precision selenium donors of variable strength.

7. Carbonyl Activation by Selenium- and Tellurium-Based Chalcogen Bonding in a Michael Addition Reaction.

8. Chalcogen Bonding Catalysis of a Nitro-Michael Reaction.

9. Catalytic Carbon-Chlorine Bond Activation by Selenium-Based Chalcogen Bond Donors.

10. Comparative Strengths of Tetrel, Pnicogen, Chalcogen, and Halogen Bonds and Contributing Factors.