TY  - JOUR
AU  - Wild, Stefan
AU  - Fickert, Michael
AU  - Mitrović, Aleksandra D.
AU  - Lloret, Vicent
AU  - Neiss, Christian
AU  - Vidal‐Moya, Jose Alejandro
AU  - Rivero‐Crespo, Miguel Angel
AU  - Leyva‐Pérez, Antonio
AU  - Werbach, Katharina
AU  - Peterlik, Herwig
AU  - Grabau, Mathias
AU  - Wittkämper, Haiko
AU  - Papp, Christian
AU  - Steinrück, Hans-Peter
AU  - Pichler, Thomas
AU  - Görling, Andreas
AU  - Hauke, Frank
AU  - Abellán, Gonzalo
AU  - Hirsch, Andreas
PY  - 2019
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/3936
AB  - The chemical bulk reductive covalent functionalization of thin‐layer black phosphorus (BP) using BP intercalation compounds has been developed. Through effective reductive activation, covalent functionalization of the charged BP by reaction with organic alkyl halides is achieved. Functionalization was extensively demonstrated by means of several spectroscopic techniques and DFT calculations; the products showed higher functionalization degrees than those obtained by neutral routes
PB  - Wiley
T2  - Angewandte Chemie International Edition
T1  - Lattice Opening upon Bulk Reductive Covalent Functionalization of Black Phosphorus
VL  - 58
IS  - 17
SP  - 5763
EP  - 5768
DO  - 10.1002/anie.201811181
ER  - 

@article{
author = "Wild, Stefan and Fickert, Michael and Mitrović, Aleksandra D. and Lloret, Vicent and Neiss, Christian and Vidal‐Moya, Jose Alejandro and Rivero‐Crespo, Miguel Angel and Leyva‐Pérez, Antonio and Werbach, Katharina and Peterlik, Herwig and Grabau, Mathias and Wittkämper, Haiko and Papp, Christian and Steinrück, Hans-Peter and Pichler, Thomas and Görling, Andreas and Hauke, Frank and Abellán, Gonzalo and Hirsch, Andreas",
year = "2019",
abstract = "The chemical bulk reductive covalent functionalization of thin‐layer black phosphorus (BP) using BP intercalation compounds has been developed. Through effective reductive activation, covalent functionalization of the charged BP by reaction with organic alkyl halides is achieved. Functionalization was extensively demonstrated by means of several spectroscopic techniques and DFT calculations; the products showed higher functionalization degrees than those obtained by neutral routes",
publisher = "Wiley",
journal = "Angewandte Chemie International Edition",
title = "Lattice Opening upon Bulk Reductive Covalent Functionalization of Black Phosphorus",
volume = "58",
number = "17",
pages = "5763-5768",
doi = "10.1002/anie.201811181"
}

Wild, S., Fickert, M., Mitrović, A. D., Lloret, V., Neiss, C., Vidal‐Moya, J. A., Rivero‐Crespo, M. A., Leyva‐Pérez, A., Werbach, K., Peterlik, H., Grabau, M., Wittkämper, H., Papp, C., Steinrück, H., Pichler, T., Görling, A., Hauke, F., Abellán, G.,& Hirsch, A.. (2019). Lattice Opening upon Bulk Reductive Covalent Functionalization of Black Phosphorus. in Angewandte Chemie International Edition
Wiley., 58(17), 5763-5768.
https://doi.org/10.1002/anie.201811181

Wild S, Fickert M, Mitrović AD, Lloret V, Neiss C, Vidal‐Moya JA, Rivero‐Crespo MA, Leyva‐Pérez A, Werbach K, Peterlik H, Grabau M, Wittkämper H, Papp C, Steinrück H, Pichler T, Görling A, Hauke F, Abellán G, Hirsch A. Lattice Opening upon Bulk Reductive Covalent Functionalization of Black Phosphorus. in Angewandte Chemie International Edition. 2019;58(17):5763-5768.
doi:10.1002/anie.201811181 .

Wild, Stefan, Fickert, Michael, Mitrović, Aleksandra D., Lloret, Vicent, Neiss, Christian, Vidal‐Moya, Jose Alejandro, Rivero‐Crespo, Miguel Angel, Leyva‐Pérez, Antonio, Werbach, Katharina, Peterlik, Herwig, Grabau, Mathias, Wittkämper, Haiko, Papp, Christian, Steinrück, Hans-Peter, Pichler, Thomas, Görling, Andreas, Hauke, Frank, Abellán, Gonzalo, Hirsch, Andreas, "Lattice Opening upon Bulk Reductive Covalent Functionalization of Black Phosphorus" in Angewandte Chemie International Edition, 58, no. 17 (2019):5763-5768,
https://doi.org/10.1002/anie.201811181 . .

TY  - JOUR
AU  - Chamberlain, Thomas W.
AU  - Pfeiffer, Rudolf
AU  - Howells, Jonathan
AU  - Peterlik, Herwig
AU  - Kuzmany, Hans
AU  - Kraeutler, Bernhard
AU  - Da Ros, Tatiana
AU  - Melle-Franco, Manuel
AU  - Zerbetto, Francesco
AU  - Milić, Dragana
AU  - Khlobystov, Andrei N.
PY  - 2012
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/1550
AB  - A range of mono- and bis-functionalised fullerenes have been synthesised and inserted into single-walled carbon nanotubes. The effect of the size and shape of the functional groups of the fullerenes on the resultant 1D arrays formed within the nanotubes was investigated by high resolution transmission electron microscopy and X-ray diffraction. The addition of non-planar, sterically bulky chains to the fullerene cage results in highly ordered 1D structures in which the fullerenes are evenly spaced along the internal nanotube cavity. Theoretical calculations reveal that the functional groups interact with neighbouring fullerene cages to space the fullerenes evenly within the confines of the nanotube. The addition of two functional groups to opposite sides of the fullerene cages results in a further increase in the separation of the fullerene cages within the nanotubes at the cost of lower nanotube filling rates.
PB  - Royal Soc Chemistry, Cambridge
T2  - Nanoscale
T1  - Engineering molecular chains in carbon nanotubes
VL  - 4
IS  - 23
SP  - 7540
EP  - 7548
DO  - 10.1039/c2nr32571c
ER  - 

@article{
author = "Chamberlain, Thomas W. and Pfeiffer, Rudolf and Howells, Jonathan and Peterlik, Herwig and Kuzmany, Hans and Kraeutler, Bernhard and Da Ros, Tatiana and Melle-Franco, Manuel and Zerbetto, Francesco and Milić, Dragana and Khlobystov, Andrei N.",
year = "2012",
abstract = "A range of mono- and bis-functionalised fullerenes have been synthesised and inserted into single-walled carbon nanotubes. The effect of the size and shape of the functional groups of the fullerenes on the resultant 1D arrays formed within the nanotubes was investigated by high resolution transmission electron microscopy and X-ray diffraction. The addition of non-planar, sterically bulky chains to the fullerene cage results in highly ordered 1D structures in which the fullerenes are evenly spaced along the internal nanotube cavity. Theoretical calculations reveal that the functional groups interact with neighbouring fullerene cages to space the fullerenes evenly within the confines of the nanotube. The addition of two functional groups to opposite sides of the fullerene cages results in a further increase in the separation of the fullerene cages within the nanotubes at the cost of lower nanotube filling rates.",
publisher = "Royal Soc Chemistry, Cambridge",
journal = "Nanoscale",
title = "Engineering molecular chains in carbon nanotubes",
volume = "4",
number = "23",
pages = "7540-7548",
doi = "10.1039/c2nr32571c"
}

Chamberlain, T. W., Pfeiffer, R., Howells, J., Peterlik, H., Kuzmany, H., Kraeutler, B., Da Ros, T., Melle-Franco, M., Zerbetto, F., Milić, D.,& Khlobystov, A. N.. (2012). Engineering molecular chains in carbon nanotubes. in Nanoscale
Royal Soc Chemistry, Cambridge., 4(23), 7540-7548.
https://doi.org/10.1039/c2nr32571c

Chamberlain TW, Pfeiffer R, Howells J, Peterlik H, Kuzmany H, Kraeutler B, Da Ros T, Melle-Franco M, Zerbetto F, Milić D, Khlobystov AN. Engineering molecular chains in carbon nanotubes. in Nanoscale. 2012;4(23):7540-7548.
doi:10.1039/c2nr32571c .

Chamberlain, Thomas W., Pfeiffer, Rudolf, Howells, Jonathan, Peterlik, Herwig, Kuzmany, Hans, Kraeutler, Bernhard, Da Ros, Tatiana, Melle-Franco, Manuel, Zerbetto, Francesco, Milić, Dragana, Khlobystov, Andrei N., "Engineering molecular chains in carbon nanotubes" in Nanoscale, 4, no. 23 (2012):7540-7548,
https://doi.org/10.1039/c2nr32571c . .