---
OA_place: publisher
OA_type: hybrid
_id: '20755'
abstract:
- lang: eng
  text: We report the development of a continuous flow approach to nitrogen atom insertion.
    The setup is modular, enabling the rapid optimization of reaction conditions for
    a wide range of substrates. The milder reaction conditions led to an improved
    substrate scope and functional group tolerance compared to batch conditions. The
    reactions can also be safely scaled up to preparative scale.
article_processing_charge: Yes (in subscription journal)
article_type: original
author:
- first_name: Sooyeon
  full_name: Moon, Sooyeon
  last_name: Moon
- first_name: Julia
  full_name: Reisenbauer, Julia
  id: 51d862e9-36ee-11f0-86d3-8534c85a5496
  last_name: Reisenbauer
- first_name: Ann-Sophie K.
  full_name: Paschke, Ann-Sophie K.
  last_name: Paschke
- first_name: Alessandro
  full_name: Scotto, Alessandro
  last_name: Scotto
- first_name: Luca
  full_name: Terraneo, Luca
  last_name: Terraneo
- first_name: Niklas
  full_name: Brenner, Niklas
  last_name: Brenner
- first_name: Quentin
  full_name: Lefebvre, Quentin
  last_name: Lefebvre
- first_name: Thomas C.
  full_name: Fessard, Thomas C.
  last_name: Fessard
- first_name: Bill
  full_name: Morandi, Bill
  last_name: Morandi
citation:
  ama: Moon S, Reisenbauer J, Paschke A-SK, et al. Efficient optimization and synthesis
    of diverse azaarenes via nitrogen atom insertion under continuous flow conditions.
    <i>Chemical Communications</i>. 2025;61(87):16993-16996. doi:<a href="https://doi.org/10.1039/d5cc03194j">10.1039/d5cc03194j</a>
  apa: Moon, S., Reisenbauer, J., Paschke, A.-S. K., Scotto, A., Terraneo, L., Brenner,
    N., … Morandi, B. (2025). Efficient optimization and synthesis of diverse azaarenes
    via nitrogen atom insertion under continuous flow conditions. <i>Chemical Communications</i>.
    Royal Society of Chemistry. <a href="https://doi.org/10.1039/d5cc03194j">https://doi.org/10.1039/d5cc03194j</a>
  chicago: Moon, Sooyeon, Julia Reisenbauer, Ann-Sophie K. Paschke, Alessandro Scotto,
    Luca Terraneo, Niklas Brenner, Quentin Lefebvre, Thomas C. Fessard, and Bill Morandi.
    “Efficient Optimization and Synthesis of Diverse Azaarenes via Nitrogen Atom Insertion
    under Continuous Flow Conditions.” <i>Chemical Communications</i>. Royal Society
    of Chemistry, 2025. <a href="https://doi.org/10.1039/d5cc03194j">https://doi.org/10.1039/d5cc03194j</a>.
  ieee: S. Moon <i>et al.</i>, “Efficient optimization and synthesis of diverse azaarenes
    via nitrogen atom insertion under continuous flow conditions,” <i>Chemical Communications</i>,
    vol. 61, no. 87. Royal Society of Chemistry, pp. 16993–16996, 2025.
  ista: Moon S, Reisenbauer J, Paschke A-SK, Scotto A, Terraneo L, Brenner N, Lefebvre
    Q, Fessard TC, Morandi B. 2025. Efficient optimization and synthesis of diverse
    azaarenes via nitrogen atom insertion under continuous flow conditions. Chemical
    Communications. 61(87), 16993–16996.
  mla: Moon, Sooyeon, et al. “Efficient Optimization and Synthesis of Diverse Azaarenes
    via Nitrogen Atom Insertion under Continuous Flow Conditions.” <i>Chemical Communications</i>,
    vol. 61, no. 87, Royal Society of Chemistry, 2025, pp. 16993–96, doi:<a href="https://doi.org/10.1039/d5cc03194j">10.1039/d5cc03194j</a>.
  short: S. Moon, J. Reisenbauer, A.-S.K. Paschke, A. Scotto, L. Terraneo, N. Brenner,
    Q. Lefebvre, T.C. Fessard, B. Morandi, Chemical Communications 61 (2025) 16993–16996.
date_created: 2025-12-09T14:22:09Z
date_published: 2025-10-06T00:00:00Z
date_updated: 2026-03-16T08:31:23Z
day: '06'
ddc:
- '540'
doi: 10.1039/d5cc03194j
extern: '1'
has_accepted_license: '1'
intvolume: '        61'
issue: '87'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.1039/D5CC03194J
month: '10'
oa: 1
oa_version: Published Version
page: 16993-16996
publication: Chemical Communications
publication_identifier:
  eissn:
  - 1364-548X
  issn:
  - 1359-7345
publication_status: published
publisher: Royal Society of Chemistry
quality_controlled: '1'
scopus_import: '1'
status: public
title: Efficient optimization and synthesis of diverse azaarenes via nitrogen atom
  insertion under continuous flow conditions
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 61
year: '2025'
...
---
OA_place: publisher
OA_type: hybrid
_id: '20757'
abstract:
- lang: eng
  text: We report the utilisation of an iodine(III) reagent to access α,β-unsaturated
    carbonyls from the corresponding silyl enol ethers and enol phosphates. The transformation
    can also be carried out in one pot, directly dehydrogenating carbonyls.
article_processing_charge: No
article_type: original
author:
- first_name: Bence B.
  full_name: Botlik, Bence B.
  last_name: Botlik
- first_name: Patrick
  full_name: Finkelstein, Patrick
  last_name: Finkelstein
- first_name: Ann-Sophie K.
  full_name: Paschke, Ann-Sophie K.
  last_name: Paschke
- first_name: Julia
  full_name: Reisenbauer, Julia
  id: 51d862e9-36ee-11f0-86d3-8534c85a5496
  last_name: Reisenbauer
- first_name: Bill
  full_name: Morandi, Bill
  last_name: Morandi
citation:
  ama: Botlik BB, Finkelstein P, Paschke A-SK, Reisenbauer J, Morandi B. Versatile
    dehydrogenation of carbonyls enabled by an iodine(III) reagent. <i>Chemical Communications</i>.
    2024;60(69):9254-9257. doi:<a href="https://doi.org/10.1039/d4cc02609h">10.1039/d4cc02609h</a>
  apa: Botlik, B. B., Finkelstein, P., Paschke, A.-S. K., Reisenbauer, J., &#38; Morandi,
    B. (2024). Versatile dehydrogenation of carbonyls enabled by an iodine(III) reagent.
    <i>Chemical Communications</i>. Royal Society of Chemistry. <a href="https://doi.org/10.1039/d4cc02609h">https://doi.org/10.1039/d4cc02609h</a>
  chicago: Botlik, Bence B., Patrick Finkelstein, Ann-Sophie K. Paschke, Julia Reisenbauer,
    and Bill Morandi. “Versatile Dehydrogenation of Carbonyls Enabled by an Iodine(III)
    Reagent.” <i>Chemical Communications</i>. Royal Society of Chemistry, 2024. <a
    href="https://doi.org/10.1039/d4cc02609h">https://doi.org/10.1039/d4cc02609h</a>.
  ieee: B. B. Botlik, P. Finkelstein, A.-S. K. Paschke, J. Reisenbauer, and B. Morandi,
    “Versatile dehydrogenation of carbonyls enabled by an iodine(III) reagent,” <i>Chemical
    Communications</i>, vol. 60, no. 69. Royal Society of Chemistry, pp. 9254–9257,
    2024.
  ista: Botlik BB, Finkelstein P, Paschke A-SK, Reisenbauer J, Morandi B. 2024. Versatile
    dehydrogenation of carbonyls enabled by an iodine(III) reagent. Chemical Communications.
    60(69), 9254–9257.
  mla: Botlik, Bence B., et al. “Versatile Dehydrogenation of Carbonyls Enabled by
    an Iodine(III) Reagent.” <i>Chemical Communications</i>, vol. 60, no. 69, Royal
    Society of Chemistry, 2024, pp. 9254–57, doi:<a href="https://doi.org/10.1039/d4cc02609h">10.1039/d4cc02609h</a>.
  short: B.B. Botlik, P. Finkelstein, A.-S.K. Paschke, J. Reisenbauer, B. Morandi,
    Chemical Communications 60 (2024) 9254–9257.
date_created: 2025-12-09T14:23:00Z
date_published: 2024-08-02T00:00:00Z
date_updated: 2025-12-16T11:19:43Z
day: '02'
doi: 10.1039/d4cc02609h
extern: '1'
external_id:
  pmid:
  - '39118590'
has_accepted_license: '1'
intvolume: '        60'
issue: '69'
language:
- iso: eng
license: https://creativecommons.org/licenses/by-nc/3.0/
main_file_link:
- open_access: '1'
  url: https://doi.org/10.1039/D4CC02609H
month: '08'
oa: 1
oa_version: Published Version
page: 9254-9257
pmid: 1
publication: Chemical Communications
publication_identifier:
  eissn:
  - 1364-548X
  issn:
  - 1359-7345
publication_status: published
publisher: Royal Society of Chemistry
quality_controlled: '1'
scopus_import: '1'
status: public
title: Versatile dehydrogenation of carbonyls enabled by an iodine(III) reagent
tmp:
  image: /images/cc_by_nc.png
  legal_code_url: https://creativecommons.org/licenses/by-nc/3.0/legalcode
  name: Creative Commons Attribution-NonCommercial 3.0 Unported (CC BY-NC 3.0)
  short: CC BY-NC (3.0)
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 60
year: '2024'
...
---
OA_place: repository
OA_type: green
_id: '17869'
abstract:
- lang: eng
  text: The formation of carbon–carbon bonds with transition metal reagents serves
    as a cornerstone of organic synthesis. Here, we show that the reactivity of an
    otherwise kinetically inert transition metal complex can be induced by an external
    electric field to affect a coupling reaction. These results highlight the importance
    of electric field effects in reaction chemistry and offers a new strategy to modulate
    organometallic reactivity.
article_processing_charge: No
article_type: letter_note
author:
- first_name: Nicholas M.
  full_name: Orchanian, Nicholas M.
  last_name: Orchanian
- first_name: Sophia
  full_name: Guizzo, Sophia
  last_name: Guizzo
- first_name: Michael L.
  full_name: Steigerwald, Michael L.
  last_name: Steigerwald
- first_name: Colin
  full_name: Nuckolls, Colin
  last_name: Nuckolls
- first_name: Latha
  full_name: Venkataraman, Latha
  id: 9ebb78a5-cc0d-11ee-8322-fae086a32caf
  last_name: Venkataraman
  orcid: 0000-0002-6957-6089
citation:
  ama: Orchanian NM, Guizzo S, Steigerwald ML, Nuckolls C, Venkataraman L. Electric-field-induced
    coupling of aryl iodides with a nickel(0) complex. <i>Chemical Communications</i>.
    2022;58(90):12556-12559. doi:<a href="https://doi.org/10.1039/d2cc03671a">10.1039/d2cc03671a</a>
  apa: Orchanian, N. M., Guizzo, S., Steigerwald, M. L., Nuckolls, C., &#38; Venkataraman,
    L. (2022). Electric-field-induced coupling of aryl iodides with a nickel(0) complex.
    <i>Chemical Communications</i>. Royal Society of Chemistry. <a href="https://doi.org/10.1039/d2cc03671a">https://doi.org/10.1039/d2cc03671a</a>
  chicago: Orchanian, Nicholas M., Sophia Guizzo, Michael L. Steigerwald, Colin Nuckolls,
    and Latha Venkataraman. “Electric-Field-Induced Coupling of Aryl Iodides with
    a Nickel(0) Complex.” <i>Chemical Communications</i>. Royal Society of Chemistry,
    2022. <a href="https://doi.org/10.1039/d2cc03671a">https://doi.org/10.1039/d2cc03671a</a>.
  ieee: N. M. Orchanian, S. Guizzo, M. L. Steigerwald, C. Nuckolls, and L. Venkataraman,
    “Electric-field-induced coupling of aryl iodides with a nickel(0) complex,” <i>Chemical
    Communications</i>, vol. 58, no. 90. Royal Society of Chemistry, pp. 12556–12559,
    2022.
  ista: Orchanian NM, Guizzo S, Steigerwald ML, Nuckolls C, Venkataraman L. 2022.
    Electric-field-induced coupling of aryl iodides with a nickel(0) complex. Chemical
    Communications. 58(90), 12556–12559.
  mla: Orchanian, Nicholas M., et al. “Electric-Field-Induced Coupling of Aryl Iodides
    with a Nickel(0) Complex.” <i>Chemical Communications</i>, vol. 58, no. 90, Royal
    Society of Chemistry, 2022, pp. 12556–59, doi:<a href="https://doi.org/10.1039/d2cc03671a">10.1039/d2cc03671a</a>.
  short: N.M. Orchanian, S. Guizzo, M.L. Steigerwald, C. Nuckolls, L. Venkataraman,
    Chemical Communications 58 (2022) 12556–12559.
date_created: 2024-09-06T13:03:38Z
date_published: 2022-10-10T00:00:00Z
date_updated: 2024-12-10T09:27:04Z
day: '10'
doi: 10.1039/d2cc03671a
extern: '1'
external_id:
  pmid:
  - '36245392'
intvolume: '        58'
issue: '90'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.26434/chemrxiv-2022-lfnw1
month: '10'
oa: 1
oa_version: Preprint
page: 12556-12559
pmid: 1
publication: Chemical Communications
publication_identifier:
  eissn:
  - 1364-548X
  issn:
  - 1359-7345
publication_status: published
publisher: Royal Society of Chemistry
quality_controlled: '1'
related_material:
  link:
  - relation: erratum
    url: https://doi.org/10.1039/d2cc03671a
scopus_import: '1'
status: public
title: Electric-field-induced coupling of aryl iodides with a nickel(0) complex
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 58
year: '2022'
...
---
_id: '13353'
abstract:
- lang: eng
  text: We show that the optical properties of indigo carmine can be modulated by
    encapsulation within a coordination cage. Depending on the host/guest molar ratio,
    the cage can predominantly encapsulate either one or two dye molecules. The 1 : 1
    complex is fluorescent, unique for an indigo dye in an aqueous solution. We have
    also found that binding two dye molecules stabilizes a previously unknown conformation
    of the cage.
article_processing_charge: No
article_type: original
author:
- first_name: Oksana
  full_name: Yanshyna, Oksana
  last_name: Yanshyna
- first_name: Liat
  full_name: Avram, Liat
  last_name: Avram
- first_name: Linda J. W.
  full_name: Shimon, Linda J. W.
  last_name: Shimon
- first_name: Rafal
  full_name: Klajn, Rafal
  id: 8e84690e-1e48-11ed-a02b-a1e6fb8bb53b
  last_name: Klajn
citation:
  ama: Yanshyna O, Avram L, Shimon LJW, Klajn R. Coexistence of 1:1 and 2:1 inclusion
    complexes of indigo carmine. <i>Chemical Communications</i>. 2022;58(21):3461-3464.
    doi:<a href="https://doi.org/10.1039/d1cc07081a">10.1039/d1cc07081a</a>
  apa: Yanshyna, O., Avram, L., Shimon, L. J. W., &#38; Klajn, R. (2022). Coexistence
    of 1:1 and 2:1 inclusion complexes of indigo carmine. <i>Chemical Communications</i>.
    Royal Society of Chemistry. <a href="https://doi.org/10.1039/d1cc07081a">https://doi.org/10.1039/d1cc07081a</a>
  chicago: Yanshyna, Oksana, Liat Avram, Linda J. W. Shimon, and Rafal Klajn. “Coexistence
    of 1:1 and 2:1 Inclusion Complexes of Indigo Carmine.” <i>Chemical Communications</i>.
    Royal Society of Chemistry, 2022. <a href="https://doi.org/10.1039/d1cc07081a">https://doi.org/10.1039/d1cc07081a</a>.
  ieee: O. Yanshyna, L. Avram, L. J. W. Shimon, and R. Klajn, “Coexistence of 1:1
    and 2:1 inclusion complexes of indigo carmine,” <i>Chemical Communications</i>,
    vol. 58, no. 21. Royal Society of Chemistry, pp. 3461–3464, 2022.
  ista: Yanshyna O, Avram L, Shimon LJW, Klajn R. 2022. Coexistence of 1:1 and 2:1
    inclusion complexes of indigo carmine. Chemical Communications. 58(21), 3461–3464.
  mla: Yanshyna, Oksana, et al. “Coexistence of 1:1 and 2:1 Inclusion Complexes of
    Indigo Carmine.” <i>Chemical Communications</i>, vol. 58, no. 21, Royal Society
    of Chemistry, 2022, pp. 3461–64, doi:<a href="https://doi.org/10.1039/d1cc07081a">10.1039/d1cc07081a</a>.
  short: O. Yanshyna, L. Avram, L.J.W. Shimon, R. Klajn, Chemical Communications 58
    (2022) 3461–3464.
date_created: 2023-08-01T09:32:55Z
date_published: 2022-01-22T00:00:00Z
date_updated: 2024-10-14T12:10:24Z
day: '22'
doi: 10.1039/d1cc07081a
extern: '1'
external_id:
  pmid:
  - '35064258'
intvolume: '        58'
issue: '21'
keyword:
- Materials Chemistry
- Metals and Alloys
- Surfaces
- Coatings and Films
- General Chemistry
- Ceramics and Composites
- Electronic
- Optical and Magnetic Materials
- Catalysis
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.1039/D1CC07081A
month: '01'
oa: 1
oa_version: Published Version
page: 3461-3464
pmid: 1
publication: Chemical Communications
publication_identifier:
  eissn:
  - 1364-548X
  issn:
  - 1359-7345
publication_status: published
publisher: Royal Society of Chemistry
quality_controlled: '1'
scopus_import: '1'
status: public
title: Coexistence of 1:1 and 2:1 inclusion complexes of indigo carmine
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 58
year: '2022'
...
---
OA_type: green
_id: '21823'
abstract:
- lang: eng
  text: DFT calculations were used to find an optimal substitution site on the triene
    backbone of a donor–acceptor Stenhouse adduct photoswitch to tune the equillibrium
    and switching kinetics of DASA without modifying the donor and acceptor groups.
    Using this approach we demonstrate a new means to tuning DASA based photoswitches
    by increasing the energy of the closed form relative to the open form. To highlight
    the potential of this approach a new DASA derivative bearing a methyl substituent
    on the 5-position of the triene was synthesized and the effect of this substitution
    was studied using 1H NMR spectroscopy, time-dependent UV-Vis and solvatochromic
    analysis. The new DASA derivative shows a higher dark equillibrium, favoring the
    open form, and drastically faster thermal recovery than the unsubstituted derivative
    with the same donor and acceptor.
article_processing_charge: No
article_type: original
author:
- first_name: Julie A.
  full_name: Peterson, Julie A.
  last_name: Peterson
- first_name: Friedrich J
  full_name: Stricker, Friedrich J
  id: 7aca2cfc-46cf-11f0-abd3-8c96b5186745
  last_name: Stricker
- first_name: Javier
  full_name: Read de Alaniz, Javier
  last_name: Read de Alaniz
citation:
  ama: Peterson JA, Stricker FJ, Read de Alaniz J. Improving the kinetics and dark
    equilibrium of donor-acceptor Stenhouse adduct by triene backbone design. <i>Chemical
    Communications</i>. 2022;58(14):2303-2306. doi:<a href="https://doi.org/10.1039/d1cc06235b">10.1039/d1cc06235b</a>
  apa: Peterson, J. A., Stricker, F. J., &#38; Read de Alaniz, J. (2022). Improving
    the kinetics and dark equilibrium of donor-acceptor Stenhouse adduct by triene
    backbone design. <i>Chemical Communications</i>. Royal Society of Chemistry. <a
    href="https://doi.org/10.1039/d1cc06235b">https://doi.org/10.1039/d1cc06235b</a>
  chicago: Peterson, Julie A., Friedrich J Stricker, and Javier Read de Alaniz. “Improving
    the Kinetics and Dark Equilibrium of Donor-Acceptor Stenhouse Adduct by Triene
    Backbone Design.” <i>Chemical Communications</i>. Royal Society of Chemistry,
    2022. <a href="https://doi.org/10.1039/d1cc06235b">https://doi.org/10.1039/d1cc06235b</a>.
  ieee: J. A. Peterson, F. J. Stricker, and J. Read de Alaniz, “Improving the kinetics
    and dark equilibrium of donor-acceptor Stenhouse adduct by triene backbone design,”
    <i>Chemical Communications</i>, vol. 58, no. 14. Royal Society of Chemistry, pp.
    2303–2306, 2022.
  ista: Peterson JA, Stricker FJ, Read de Alaniz J. 2022. Improving the kinetics and
    dark equilibrium of donor-acceptor Stenhouse adduct by triene backbone design.
    Chemical Communications. 58(14), 2303–2306.
  mla: Peterson, Julie A., et al. “Improving the Kinetics and Dark Equilibrium of
    Donor-Acceptor Stenhouse Adduct by Triene Backbone Design.” <i>Chemical Communications</i>,
    vol. 58, no. 14, Royal Society of Chemistry, 2022, pp. 2303–06, doi:<a href="https://doi.org/10.1039/d1cc06235b">10.1039/d1cc06235b</a>.
  short: J.A. Peterson, F.J. Stricker, J. Read de Alaniz, Chemical Communications
    58 (2022) 2303–2306.
date_created: 2026-05-06T10:59:03Z
date_published: 2022-01-17T00:00:00Z
date_updated: 2026-05-18T09:46:30Z
day: '17'
ddc:
- '540'
doi: 10.1039/d1cc06235b
extern: '1'
external_id:
  pmid:
  - '35075464'
intvolume: '        58'
issue: '14'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.1039/D1CC06235B
month: '01'
oa: 1
oa_version: Accepted Version
page: 2303-2306
pmid: 1
publication: Chemical Communications
publication_identifier:
  eissn:
  - 1364-548X
  issn:
  - 1359-7345
publication_status: published
publisher: Royal Society of Chemistry
quality_controlled: '1'
scopus_import: '1'
status: public
title: Improving the kinetics and dark equilibrium of donor-acceptor Stenhouse adduct
  by triene backbone design
type: journal_article
user_id: ba8df636-2132-11f1-aed0-ed93e2281fdd
volume: 58
year: '2022'
...
---
OA_type: closed access
_id: '17901'
abstract:
- lang: eng
  text: A 1,1,2,2-tetrakis(4-aminophenyl)ethene with three paths of π-conjugation,
    linear-cis, linear-trans and a cross-conjugation, has been prepared. The molecule
    is able to bind to gold electrodes forming molecular junctions for single-molecule
    conductance measurements. Only two regimes of conduction are found experimentally.
    The modelling of the conductance allows to assign them to through-bond transmission
    in the linear case, while the cross-conjugated channel is further assisted by
    through-space transmission, partially alleviating the destructive quantum interference.
article_processing_charge: No
article_type: original
author:
- first_name: Samara
  full_name: Medina Rivero, Samara
  last_name: Medina Rivero
- first_name: Paloma
  full_name: García Arroyo, Paloma
  last_name: García Arroyo
- first_name: Liang
  full_name: Li, Liang
  last_name: Li
- first_name: Suman
  full_name: Gunasekaran, Suman
  last_name: Gunasekaran
- first_name: Thijs
  full_name: Stuyver, Thijs
  last_name: Stuyver
- first_name: María José
  full_name: Mancheño, María José
  last_name: Mancheño
- first_name: Mercedes
  full_name: Alonso, Mercedes
  last_name: Alonso
- first_name: Latha
  full_name: Venkataraman, Latha
  id: 9ebb78a5-cc0d-11ee-8322-fae086a32caf
  last_name: Venkataraman
  orcid: 0000-0002-6957-6089
- first_name: José L.
  full_name: Segura, José L.
  last_name: Segura
- first_name: Juan
  full_name: Casado, Juan
  last_name: Casado
citation:
  ama: Medina Rivero S, García Arroyo P, Li L, et al. Single-molecule conductance
    in a unique cross-conjugated tetra(aminoaryl)ethene. <i>Chemical Communications</i>.
    2021;57(5):591-594. doi:<a href="https://doi.org/10.1039/d0cc07124b">10.1039/d0cc07124b</a>
  apa: Medina Rivero, S., García Arroyo, P., Li, L., Gunasekaran, S., Stuyver, T.,
    Mancheño, M. J., … Casado, J. (2021). Single-molecule conductance in a unique
    cross-conjugated tetra(aminoaryl)ethene. <i>Chemical Communications</i>. Royal
    Society of Chemistry. <a href="https://doi.org/10.1039/d0cc07124b">https://doi.org/10.1039/d0cc07124b</a>
  chicago: Medina Rivero, Samara, Paloma García Arroyo, Liang Li, Suman Gunasekaran,
    Thijs Stuyver, María José Mancheño, Mercedes Alonso, Latha Venkataraman, José
    L. Segura, and Juan Casado. “Single-Molecule Conductance in a Unique Cross-Conjugated
    Tetra(Aminoaryl)Ethene.” <i>Chemical Communications</i>. Royal Society of Chemistry,
    2021. <a href="https://doi.org/10.1039/d0cc07124b">https://doi.org/10.1039/d0cc07124b</a>.
  ieee: S. Medina Rivero <i>et al.</i>, “Single-molecule conductance in a unique cross-conjugated
    tetra(aminoaryl)ethene,” <i>Chemical Communications</i>, vol. 57, no. 5. Royal
    Society of Chemistry, pp. 591–594, 2021.
  ista: Medina Rivero S, García Arroyo P, Li L, Gunasekaran S, Stuyver T, Mancheño
    MJ, Alonso M, Venkataraman L, Segura JL, Casado J. 2021. Single-molecule conductance
    in a unique cross-conjugated tetra(aminoaryl)ethene. Chemical Communications.
    57(5), 591–594.
  mla: Medina Rivero, Samara, et al. “Single-Molecule Conductance in a Unique Cross-Conjugated
    Tetra(Aminoaryl)Ethene.” <i>Chemical Communications</i>, vol. 57, no. 5, Royal
    Society of Chemistry, 2021, pp. 591–94, doi:<a href="https://doi.org/10.1039/d0cc07124b">10.1039/d0cc07124b</a>.
  short: S. Medina Rivero, P. García Arroyo, L. Li, S. Gunasekaran, T. Stuyver, M.J.
    Mancheño, M. Alonso, L. Venkataraman, J.L. Segura, J. Casado, Chemical Communications
    57 (2021) 591–594.
date_created: 2024-09-09T06:44:58Z
date_published: 2021-05-01T00:00:00Z
date_updated: 2024-12-10T10:23:49Z
day: '01'
doi: 10.1039/d0cc07124b
extern: '1'
external_id:
  pmid:
  - '33325935'
intvolume: '        57'
issue: '5'
language:
- iso: eng
month: '05'
oa_version: None
page: 591-594
pmid: 1
publication: Chemical Communications
publication_identifier:
  eissn:
  - 1364-548X
  issn:
  - 1359-7345
publication_status: published
publisher: Royal Society of Chemistry
quality_controlled: '1'
scopus_import: '1'
status: public
title: Single-molecule conductance in a unique cross-conjugated tetra(aminoaryl)ethene
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 57
year: '2021'
...
---
OA_place: publisher
OA_type: hybrid
_id: '20765'
abstract:
- lang: eng
  text: <p>A cascade Suzuki–Miyaura cross-coupling between two non-symmetrical coupling
    partners gave rise to 9,10-dihydrophenanthrenes with full site-selectivity. The
    choice of base was critical to facilitate the challenging coupling of the secondary
    boronate group.</p>
article_processing_charge: No
article_type: original
author:
- first_name: Suzanne
  full_name: Willems, Suzanne
  last_name: Willems
- first_name: Georgios
  full_name: Toupalas, Georgios
  last_name: Toupalas
- first_name: Julia
  full_name: Reisenbauer, Julia
  id: 51d862e9-36ee-11f0-86d3-8534c85a5496
  last_name: Reisenbauer
- first_name: Bill
  full_name: Morandi, Bill
  last_name: Morandi
citation:
  ama: Willems S, Toupalas G, Reisenbauer J, Morandi B. A site-selective and stereospecific
    cascade Suzuki–Miyaura annulation of alkyl 1,2-bisboronic esters and 2,2′-dihalo
    1,1′-biaryls. <i>Chemical Communications</i>. 2021;57(32):3909-3912. doi:<a href="https://doi.org/10.1039/d1cc00648g">10.1039/d1cc00648g</a>
  apa: Willems, S., Toupalas, G., Reisenbauer, J., &#38; Morandi, B. (2021). A site-selective
    and stereospecific cascade Suzuki–Miyaura annulation of alkyl 1,2-bisboronic esters
    and 2,2′-dihalo 1,1′-biaryls. <i>Chemical Communications</i>. Royal Society of
    Chemistry. <a href="https://doi.org/10.1039/d1cc00648g">https://doi.org/10.1039/d1cc00648g</a>
  chicago: Willems, Suzanne, Georgios Toupalas, Julia Reisenbauer, and Bill Morandi.
    “A Site-Selective and Stereospecific Cascade Suzuki–Miyaura Annulation of Alkyl
    1,2-Bisboronic Esters and 2,2′-Dihalo 1,1′-Biaryls.” <i>Chemical Communications</i>.
    Royal Society of Chemistry, 2021. <a href="https://doi.org/10.1039/d1cc00648g">https://doi.org/10.1039/d1cc00648g</a>.
  ieee: S. Willems, G. Toupalas, J. Reisenbauer, and B. Morandi, “A site-selective
    and stereospecific cascade Suzuki–Miyaura annulation of alkyl 1,2-bisboronic esters
    and 2,2′-dihalo 1,1′-biaryls,” <i>Chemical Communications</i>, vol. 57, no. 32.
    Royal Society of Chemistry, pp. 3909–3912, 2021.
  ista: Willems S, Toupalas G, Reisenbauer J, Morandi B. 2021. A site-selective and
    stereospecific cascade Suzuki–Miyaura annulation of alkyl 1,2-bisboronic esters
    and 2,2′-dihalo 1,1′-biaryls. Chemical Communications. 57(32), 3909–3912.
  mla: Willems, Suzanne, et al. “A Site-Selective and Stereospecific Cascade Suzuki–Miyaura
    Annulation of Alkyl 1,2-Bisboronic Esters and 2,2′-Dihalo 1,1′-Biaryls.” <i>Chemical
    Communications</i>, vol. 57, no. 32, Royal Society of Chemistry, 2021, pp. 3909–12,
    doi:<a href="https://doi.org/10.1039/d1cc00648g">10.1039/d1cc00648g</a>.
  short: S. Willems, G. Toupalas, J. Reisenbauer, B. Morandi, Chemical Communications
    57 (2021) 3909–3912.
date_created: 2025-12-09T14:25:17Z
date_published: 2021-03-15T00:00:00Z
date_updated: 2025-12-16T12:06:53Z
day: '15'
ddc:
- '540'
doi: 10.1039/d1cc00648g
extern: '1'
external_id:
  pmid:
  - '33871510'
has_accepted_license: '1'
intvolume: '        57'
issue: '32'
language:
- iso: eng
license: https://creativecommons.org/licenses/by/3.0/
main_file_link:
- open_access: '1'
  url: "DOI\thttps://doi.org/10.1039/D1CC00648G"
month: '03'
oa: 1
oa_version: Published Version
page: 3909-3912
pmid: 1
publication: Chemical Communications
publication_identifier:
  eissn:
  - 1364-548X
  issn:
  - 1359-7345
publication_status: published
publisher: Royal Society of Chemistry
quality_controlled: '1'
scopus_import: '1'
status: public
title: A site-selective and stereospecific cascade Suzuki–Miyaura annulation of alkyl
  1,2-bisboronic esters and 2,2′-dihalo 1,1′-biaryls
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/3.0/legalcode
  name: Creative Commons Attribution 3.0 Unported (CC BY 3.0)
  short: CC BY (3.0)
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 57
year: '2021'
...
---
OA_type: closed access
_id: '21082'
abstract:
- lang: eng
  text: A novel chiral aromatic δ-amino acid building block was shown to fully induce
    handedness in quinoline oligoamide foldamers with the possibility of further increasing
    the bias by combining multiples of these units in the same sequence. Through its
    incorporation within the helix, both N- and C-termini are still accessible for
    further functionalisation.
article_processing_charge: No
article_type: original
author:
- first_name: Daniel
  full_name: Bindl, Daniel
  last_name: Bindl
- first_name: Elisabeth
  full_name: Heinemann, Elisabeth
  last_name: Heinemann
- first_name: Pradeep K
  full_name: Mandal, Pradeep K
  id: 6a3def15-d4b4-11ef-9fa9-a24c1f545ec3
  last_name: Mandal
  orcid: 0000-0001-5996-956X
- first_name: Ivan
  full_name: Huc, Ivan
  last_name: Huc
citation:
  ama: Bindl D, Heinemann E, Mandal PK, Huc I. Quantitative helix handedness bias
    through a single H vs. CH3 stereochemical differentiation. <i>Chemical Communications</i>.
    2021;57(46):5662-5665. doi:<a href="https://doi.org/10.1039/d1cc01452h">10.1039/d1cc01452h</a>
  apa: Bindl, D., Heinemann, E., Mandal, P. K., &#38; Huc, I. (2021). Quantitative
    helix handedness bias through a single H vs. CH3 stereochemical differentiation.
    <i>Chemical Communications</i>. Royal Society of Chemistry. <a href="https://doi.org/10.1039/d1cc01452h">https://doi.org/10.1039/d1cc01452h</a>
  chicago: Bindl, Daniel, Elisabeth Heinemann, Pradeep K Mandal, and Ivan Huc. “Quantitative
    Helix Handedness Bias through a Single H vs. CH3 Stereochemical Differentiation.”
    <i>Chemical Communications</i>. Royal Society of Chemistry, 2021. <a href="https://doi.org/10.1039/d1cc01452h">https://doi.org/10.1039/d1cc01452h</a>.
  ieee: D. Bindl, E. Heinemann, P. K. Mandal, and I. Huc, “Quantitative helix handedness
    bias through a single H vs. CH3 stereochemical differentiation,” <i>Chemical Communications</i>,
    vol. 57, no. 46. Royal Society of Chemistry, pp. 5662–5665, 2021.
  ista: Bindl D, Heinemann E, Mandal PK, Huc I. 2021. Quantitative helix handedness
    bias through a single H vs. CH3 stereochemical differentiation. Chemical Communications.
    57(46), 5662–5665.
  mla: Bindl, Daniel, et al. “Quantitative Helix Handedness Bias through a Single
    H vs. CH3 Stereochemical Differentiation.” <i>Chemical Communications</i>, vol.
    57, no. 46, Royal Society of Chemistry, 2021, pp. 5662–65, doi:<a href="https://doi.org/10.1039/d1cc01452h">10.1039/d1cc01452h</a>.
  short: D. Bindl, E. Heinemann, P.K. Mandal, I. Huc, Chemical Communications 57 (2021)
    5662–5665.
date_created: 2026-01-29T15:18:02Z
date_published: 2021-04-29T00:00:00Z
date_updated: 2026-02-20T07:01:01Z
day: '29'
doi: 10.1039/d1cc01452h
extern: '1'
external_id:
  pmid:
  - '33972976 '
has_accepted_license: '1'
intvolume: '        57'
issue: '46'
language:
- iso: eng
month: '04'
oa_version: None
page: 5662-5665
pmid: 1
publication: Chemical Communications
publication_identifier:
  eissn:
  - 1364-548X
  issn:
  - 1359-7345
publication_status: published
publisher: Royal Society of Chemistry
quality_controlled: '1'
status: public
title: Quantitative helix handedness bias through a single H vs. CH3 stereochemical
  differentiation
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 57
year: '2021'
...
---
OA_type: closed access
_id: '21100'
abstract:
- lang: eng
  text: 'Using commercial screens for crystallization of biomolecules and taking advantage
    of the use of racemic crystallography allowed the production of X-ray quality
    single crystals and the elucidation at 1.08 Å resolution of the solid state structure
    of a difficult target: the complex between glucopyranose and a water soluble macrocyclic
    receptor equipped with dendritic multianionic solubilizing chains.'
article_processing_charge: No
article_type: original
author:
- first_name: Pradeep K
  full_name: Mandal, Pradeep K
  id: 6a3def15-d4b4-11ef-9fa9-a24c1f545ec3
  last_name: Mandal
  orcid: 0000-0001-5996-956X
- first_name: Brice
  full_name: Kauffmann, Brice
  last_name: Kauffmann
- first_name: Harry
  full_name: Destecroix, Harry
  last_name: Destecroix
- first_name: Yann
  full_name: Ferrand, Yann
  last_name: Ferrand
- first_name: Anthony P.
  full_name: Davis, Anthony P.
  last_name: Davis
- first_name: Ivan
  full_name: Huc, Ivan
  last_name: Huc
citation:
  ama: Mandal PK, Kauffmann B, Destecroix H, Ferrand Y, Davis AP, Huc I. Crystal structure
    of a complex between β-glucopyranose and a macrocyclic receptor with dendritic
    multicharged water solubilizing chains. <i>Chemical Communications</i>. 2016;52(60):9355-9358.
    doi:<a href="https://doi.org/10.1039/c6cc04466b">10.1039/c6cc04466b</a>
  apa: Mandal, P. K., Kauffmann, B., Destecroix, H., Ferrand, Y., Davis, A. P., &#38;
    Huc, I. (2016). Crystal structure of a complex between β-glucopyranose and a macrocyclic
    receptor with dendritic multicharged water solubilizing chains. <i>Chemical Communications</i>.
    Royal Society of Chemistry. <a href="https://doi.org/10.1039/c6cc04466b">https://doi.org/10.1039/c6cc04466b</a>
  chicago: Mandal, Pradeep K, Brice Kauffmann, Harry Destecroix, Yann Ferrand, Anthony
    P. Davis, and Ivan Huc. “Crystal Structure of a Complex between β-Glucopyranose
    and a Macrocyclic Receptor with Dendritic Multicharged Water Solubilizing Chains.”
    <i>Chemical Communications</i>. Royal Society of Chemistry, 2016. <a href="https://doi.org/10.1039/c6cc04466b">https://doi.org/10.1039/c6cc04466b</a>.
  ieee: P. K. Mandal, B. Kauffmann, H. Destecroix, Y. Ferrand, A. P. Davis, and I.
    Huc, “Crystal structure of a complex between β-glucopyranose and a macrocyclic
    receptor with dendritic multicharged water solubilizing chains,” <i>Chemical Communications</i>,
    vol. 52, no. 60. Royal Society of Chemistry, pp. 9355–9358, 2016.
  ista: Mandal PK, Kauffmann B, Destecroix H, Ferrand Y, Davis AP, Huc I. 2016. Crystal
    structure of a complex between β-glucopyranose and a macrocyclic receptor with
    dendritic multicharged water solubilizing chains. Chemical Communications. 52(60),
    9355–9358.
  mla: Mandal, Pradeep K., et al. “Crystal Structure of a Complex between β-Glucopyranose
    and a Macrocyclic Receptor with Dendritic Multicharged Water Solubilizing Chains.”
    <i>Chemical Communications</i>, vol. 52, no. 60, Royal Society of Chemistry, 2016,
    pp. 9355–58, doi:<a href="https://doi.org/10.1039/c6cc04466b">10.1039/c6cc04466b</a>.
  short: P.K. Mandal, B. Kauffmann, H. Destecroix, Y. Ferrand, A.P. Davis, I. Huc,
    Chemical Communications 52 (2016) 9355–9358.
date_created: 2026-01-29T21:42:03Z
date_published: 2016-06-28T00:00:00Z
date_updated: 2026-02-23T09:18:46Z
day: '28'
doi: 10.1039/c6cc04466b
extern: '1'
has_accepted_license: '1'
intvolume: '        52'
issue: '60'
language:
- iso: eng
month: '06'
oa_version: None
page: 9355-9358
publication: Chemical Communications
publication_identifier:
  eissn:
  - 1364-548X
  issn:
  - 1359-7345
publication_status: published
publisher: Royal Society of Chemistry
quality_controlled: '1'
status: public
title: Crystal structure of a complex between β-glucopyranose and a macrocyclic receptor
  with dendritic multicharged water solubilizing chains
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 52
year: '2016'
...
---
_id: '13395'
abstract:
- lang: eng
  text: Metallic nanoparticles co-functionalised with monolayers of UV- and CO2-sensitive
    ligands were prepared and shown to respond to these two types of stimuli reversibly
    and in an orthogonal fashion. The composition of the coating could be tailored
    to yield nanoparticles capable of aggregating exclusively when both UV and CO2
    were applied at the same time, analogously to the behaviour of an AND logic gate.
article_processing_charge: No
article_type: original
author:
- first_name: Ji-Woong
  full_name: Lee, Ji-Woong
  last_name: Lee
- first_name: Rafal
  full_name: Klajn, Rafal
  id: 8e84690e-1e48-11ed-a02b-a1e6fb8bb53b
  last_name: Klajn
citation:
  ama: Lee J-W, Klajn R. Dual-responsive nanoparticles that aggregate under the simultaneous
    action of light and CO2. <i>Chemical Communications</i>. 2015;51(11):2036-2039.
    doi:<a href="https://doi.org/10.1039/c4cc08541h">10.1039/c4cc08541h</a>
  apa: Lee, J.-W., &#38; Klajn, R. (2015). Dual-responsive nanoparticles that aggregate
    under the simultaneous action of light and CO2. <i>Chemical Communications</i>.
    Royal Society of Chemistry. <a href="https://doi.org/10.1039/c4cc08541h">https://doi.org/10.1039/c4cc08541h</a>
  chicago: Lee, Ji-Woong, and Rafal Klajn. “Dual-Responsive Nanoparticles That Aggregate
    under the Simultaneous Action of Light and CO2.” <i>Chemical Communications</i>.
    Royal Society of Chemistry, 2015. <a href="https://doi.org/10.1039/c4cc08541h">https://doi.org/10.1039/c4cc08541h</a>.
  ieee: J.-W. Lee and R. Klajn, “Dual-responsive nanoparticles that aggregate under
    the simultaneous action of light and CO2,” <i>Chemical Communications</i>, vol.
    51, no. 11. Royal Society of Chemistry, pp. 2036–2039, 2015.
  ista: Lee J-W, Klajn R. 2015. Dual-responsive nanoparticles that aggregate under
    the simultaneous action of light and CO2. Chemical Communications. 51(11), 2036–2039.
  mla: Lee, Ji-Woong, and Rafal Klajn. “Dual-Responsive Nanoparticles That Aggregate
    under the Simultaneous Action of Light and CO2.” <i>Chemical Communications</i>,
    vol. 51, no. 11, Royal Society of Chemistry, 2015, pp. 2036–39, doi:<a href="https://doi.org/10.1039/c4cc08541h">10.1039/c4cc08541h</a>.
  short: J.-W. Lee, R. Klajn, Chemical Communications 51 (2015) 2036–2039.
date_created: 2023-08-01T09:44:48Z
date_published: 2015-11-18T00:00:00Z
date_updated: 2024-10-14T12:17:58Z
day: '18'
doi: 10.1039/c4cc08541h
extern: '1'
external_id:
  pmid:
  - '25417754'
intvolume: '        51'
issue: '11'
keyword:
- Materials Chemistry
- Metals and Alloys
- Surfaces
- Coatings and Films
- General Chemistry
- Ceramics and Composites
- Electronic
- Optical and Magnetic Materials
- Catalysis
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.1039/C4CC08541H
month: '11'
oa: 1
oa_version: Published Version
page: 2036-2039
pmid: 1
publication: Chemical Communications
publication_identifier:
  eissn:
  - 1364-548X
  issn:
  - 1359-7345
publication_status: published
publisher: Royal Society of Chemistry
quality_controlled: '1'
scopus_import: '1'
status: public
title: Dual-responsive nanoparticles that aggregate under the simultaneous action
  of light and CO2
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 51
year: '2015'
...