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Showing 1 to 12 of 143 entries
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[Psychotherapy--dynamic or not].

Lakartidningen

Ottosson JO.
PMID: 1128127
Lakartidningen. 1975 May 21;72(21):2278-80.

No abstract available.

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Ottosson JO. Psykoterapi--dynamisk eller inte [Psychotherapy--dynamic or not]. Lakartidningen. 1975;72(21):2278-80
Ottosson, J. O. (1975). Psykoterapi--dynamisk eller inte [Psychotherapy--dynamic or not]. Lakartidningen, 72(21), 2278-80.
Ottosson, J O. "Psykoterapi--dynamisk eller inte" [Psychotherapy--dynamic or not]. Lakartidningen vol. 72,21 (1975): 2278-80.
Ottosson JO. Psykoterapi--dynamisk eller inte [Psychotherapy--dynamic or not]. Lakartidningen. 1975 May 21;72(21):2278-80. Swedish. PMID: 1128127.
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Excited state aromaticity and antiaromaticity: opportunities for photophysical and photochemical rationalizations.

Chemical reviews

Rosenberg M, Dahlstrand C, Kilså K, Ottosson H.
PMID: 24712859
Chem Rev. 2014 May 28;114(10):5379-425. doi: 10.1021/cr300471v. Epub 2014 Apr 08.

No abstract available.

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Rosenberg M, Dahlstrand C, Kilså K, et al. Excited state aromaticity and antiaromaticity: opportunities for photophysical and photochemical rationalizations. Chem Rev. 2014;114(10):5379-425doi: 10.1021/cr300471v.
Rosenberg, M., Dahlstrand, C., Kilså, K., & Ottosson, H. (2014). Excited state aromaticity and antiaromaticity: opportunities for photophysical and photochemical rationalizations. Chemical reviews, 114(10), 5379-425. https://doi.org/10.1021/cr300471v
Rosenberg, Martin, et al. "Excited state aromaticity and antiaromaticity: opportunities for photophysical and photochemical rationalizations." Chemical reviews vol. 114,10 (2014): 5379-425. doi: https://doi.org/10.1021/cr300471v
Rosenberg M, Dahlstrand C, Kilså K, Ottosson H. Excited state aromaticity and antiaromaticity: opportunities for photophysical and photochemical rationalizations. Chem Rev. 2014 May 28;114(10):5379-425. doi: 10.1021/cr300471v. Epub 2014 Apr 08. PMID: 24712859.
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Nano-fabrication of molecular electronic junctions by targeted modification of metal-molecule bonds.

Scientific reports

Jafri SH, Löfås H, Blom T, Wallner A, Grigoriev A, Ahuja R, Ottosson H, Leifer K.
PMID: 26395225
Sci Rep. 2015 Sep 23;5:14431. doi: 10.1038/srep14431.

Reproducibility, stability and the coupling between electrical and molecular properties are central challenges in the field of molecular electronics. The field not only needs devices that fulfill these criteria but they also need to be up-scalable to application size....

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Jafri SH, Löfås H, Blom T, et al. Nano-fabrication of molecular electronic junctions by targeted modification of metal-molecule bonds. Sci Rep. 2015;5:14431doi: 10.1038/srep14431.
Jafri, S. H., Löfås, H., Blom, T., Wallner, A., Grigoriev, A., Ahuja, R., Ottosson, H., & Leifer, K. (2015). Nano-fabrication of molecular electronic junctions by targeted modification of metal-molecule bonds. Scientific reports, 514431. https://doi.org/10.1038/srep14431
Jafri, S Hassan M, et al. "Nano-fabrication of molecular electronic junctions by targeted modification of metal-molecule bonds." Scientific reports vol. 5 (2015): 14431. doi: https://doi.org/10.1038/srep14431
Jafri SH, Löfås H, Blom T, Wallner A, Grigoriev A, Ahuja R, Ottosson H, Leifer K. Nano-fabrication of molecular electronic junctions by targeted modification of metal-molecule bonds. Sci Rep. 2015 Sep 23;5:14431. doi: 10.1038/srep14431. PMID: 26395225; PMCID: PMC5155674.
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Many-body effects and excitonic features in 2D biphenylene carbon.

The Journal of chemical physics

Lüder J, Puglia C, Ottosson H, Eriksson O, Sanyal B, Brena B.
PMID: 26772582
J Chem Phys. 2016 Jan 14;144(2):024702. doi: 10.1063/1.4939273.

The remarkable excitonic effects in low dimensional materials in connection to large binding energies of excitons are of great importance for research and technological applications such as in solar energy and quantum information processing as well as for fundamental...

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Lüder J, Puglia C, Ottosson H, et al. Many-body effects and excitonic features in 2D biphenylene carbon. J Chem Phys. 2016;144(2):024702doi: 10.1063/1.4939273.
Lüder, J., Puglia, C., Ottosson, H., Eriksson, O., Sanyal, B., & Brena, B. (2016). Many-body effects and excitonic features in 2D biphenylene carbon. The Journal of chemical physics, 144(2), 024702. https://doi.org/10.1063/1.4939273
Lüder, Johann, et al. "Many-body effects and excitonic features in 2D biphenylene carbon." The Journal of chemical physics vol. 144,2 (2016): 024702. doi: https://doi.org/10.1063/1.4939273
Lüder J, Puglia C, Ottosson H, Eriksson O, Sanyal B, Brena B. Many-body effects and excitonic features in 2D biphenylene carbon. J Chem Phys. 2016 Jan 14;144(2):024702. doi: 10.1063/1.4939273. PMID: 26772582.
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The Missing C1-C5 Cycloaromatization Reaction: Triplet State Antiaromaticity Relief and Self-Terminating Photorelease of Formaldehyde for Synthesis of Fulvenes from Enynes.

Journal of the American Chemical Society

Mohamed RK, Mondal S, Jorner K, Delgado TF, Lobodin VV, Ottosson H, Alabugin IV.
PMID: 26536479
J Am Chem Soc. 2015 Dec 16;137(49):15441-50. doi: 10.1021/jacs.5b07448. Epub 2015 Dec 03.

The last missing example of the four archetypical cycloaromatizations of enediynes and enynes was discovered by combining a twisted alkene excited state with a new self-terminating path for intramolecular conversion of diradicals into closed-shell products. Photoexcitation of aromatic enynes...

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Mohamed RK, Mondal S, Jorner K, et al. The Missing C1-C5 Cycloaromatization Reaction: Triplet State Antiaromaticity Relief and Self-Terminating Photorelease of Formaldehyde for Synthesis of Fulvenes from Enynes. J Am Chem Soc. 2015;137(49):15441-50doi: 10.1021/jacs.5b07448.
Mohamed, R. K., Mondal, S., Jorner, K., Delgado, T. F., Lobodin, V. V., Ottosson, H., & Alabugin, I. V. (2015). The Missing C1-C5 Cycloaromatization Reaction: Triplet State Antiaromaticity Relief and Self-Terminating Photorelease of Formaldehyde for Synthesis of Fulvenes from Enynes. Journal of the American Chemical Society, 137(49), 15441-50. https://doi.org/10.1021/jacs.5b07448
Mohamed, Rana K, et al. "The Missing C1-C5 Cycloaromatization Reaction: Triplet State Antiaromaticity Relief and Self-Terminating Photorelease of Formaldehyde for Synthesis of Fulvenes from Enynes." Journal of the American Chemical Society vol. 137,49 (2015): 15441-50. doi: https://doi.org/10.1021/jacs.5b07448
Mohamed RK, Mondal S, Jorner K, Delgado TF, Lobodin VV, Ottosson H, Alabugin IV. The Missing C1-C5 Cycloaromatization Reaction: Triplet State Antiaromaticity Relief and Self-Terminating Photorelease of Formaldehyde for Synthesis of Fulvenes from Enynes. J Am Chem Soc. 2015 Dec 16;137(49):15441-50. doi: 10.1021/jacs.5b07448. Epub 2015 Dec 03. PMID: 26536479.
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Analysis of a Compound Class with Triplet States Stabilized by Potentially Baird Aromatic [10]Annulenyl Dicationic Rings.

Chemistry (Weinheim an der Bergstrasse, Germany)

Jorner K, Feixas F, Ayub R, Lindh R, Solà M, Ottosson H.
PMID: 26791436
Chemistry. 2016 Feb 18;22(8):2793-800. doi: 10.1002/chem.201504924. Epub 2016 Jan 21.

The low-lying triplet state of a recently published compound (TMTQ) was analyzed quantum chemically in light of suggestions that it is influenced by Baird aromaticity. Two mesomeric structures describe this state: 1) a zwitterionic Baird aromatic structure with a...

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Jorner K, Feixas F, Ayub R, et al. Analysis of a Compound Class with Triplet States Stabilized by Potentially Baird Aromatic [10]Annulenyl Dicationic Rings. Chemistry. 2016;22(8):2793-800doi: 10.1002/chem.201504924.
Jorner, K., Feixas, F., Ayub, R., Lindh, R., Solà, M., & Ottosson, H. (2016). Analysis of a Compound Class with Triplet States Stabilized by Potentially Baird Aromatic [10]Annulenyl Dicationic Rings. Chemistry (Weinheim an der Bergstrasse, Germany), 22(8), 2793-800. https://doi.org/10.1002/chem.201504924
Jorner, Kjell, et al. "Analysis of a Compound Class with Triplet States Stabilized by Potentially Baird Aromatic [10]Annulenyl Dicationic Rings." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 22,8 (2016): 2793-800. doi: https://doi.org/10.1002/chem.201504924
Jorner K, Feixas F, Ayub R, Lindh R, Solà M, Ottosson H. Analysis of a Compound Class with Triplet States Stabilized by Potentially Baird Aromatic [10]Annulenyl Dicationic Rings. Chemistry. 2016 Feb 18;22(8):2793-800. doi: 10.1002/chem.201504924. Epub 2016 Jan 21. PMID: 26791436.
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[Methodical education for training of specialists in psychiatry: How to organize national courses of lectures].

Lakartidningen

Ottosson JO.
PMID: 5597585
Lakartidningen. 1967 Jul 12;64(28):2800-8.

No abstract available.

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Ottosson JO. Systematisk undervisning under specialistubildningen i psykiatri: Förslag till organisation av rikskurser. [Methodical education for training of specialists in psychiatry: How to organize national courses of lectures]. Lakartidningen. 1967;64(28):2800-8
Ottosson, J. O. (1967). Systematisk undervisning under specialistubildningen i psykiatri: Förslag till organisation av rikskurser. [Methodical education for training of specialists in psychiatry: How to organize national courses of lectures]. Lakartidningen, 64(28), 2800-8.
Ottosson, J O. "Systematisk undervisning under specialistubildningen i psykiatri: Förslag till organisation av rikskurser." [Methodical education for training of specialists in psychiatry: How to organize national courses of lectures]. Lakartidningen vol. 64,28 (1967): 2800-8.
Ottosson JO. Systematisk undervisning under specialistubildningen i psykiatri: Förslag till organisation av rikskurser. [Methodical education for training of specialists in psychiatry: How to organize national courses of lectures]. Lakartidningen. 1967 Jul 12;64(28):2800-8. Swedish. PMID: 5597585.
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Is Unilateral Nondominant ECT as Efficient as Bilateral ECT? A New Look at the Evidence.

Convulsive therapy

Ottosson JO.
PMID: 11941122
Convuls Ther. 1991;7(3):190-200.

A survey of 24 comparisons of the antidepressive efficiency of bilateral and unilateral nondominant electroconvulsive therapy (ECT), fulfilling strict methodological criteria, shows a preponderance of studies in favor of bilateral ECT. However, the inferiority of unilateral nondominant ECT can...

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Ottosson JO. Is Unilateral Nondominant ECT as Efficient as Bilateral ECT? A New Look at the Evidence. Convuls Ther. 1991;7(3):190-200
Ottosson, J. O. (1991). Is Unilateral Nondominant ECT as Efficient as Bilateral ECT? A New Look at the Evidence. Convulsive therapy, 7(3), 190-200.
Ottosson, Jan-Otto. "Is Unilateral Nondominant ECT as Efficient as Bilateral ECT? A New Look at the Evidence." Convulsive therapy vol. 7,3 (1991): 190-200.
Ottosson JO. Is Unilateral Nondominant ECT as Efficient as Bilateral ECT? A New Look at the Evidence. Convuls Ther. 1991;7(3):190-200. PMID: 11941122.
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Z/E-photoisomerizations of olefins with 4npi- or (4n + 2)pi-electron substituents: zigzag variations in olefin properties along the T(1) state energy surfaces.

The Journal of organic chemistry

Kato H, Brink M, Möllerstedt H, Piqueras MC, Crespo R, Ottosson H.
PMID: 16268625
J Org Chem. 2005 Nov 11;70(23):9495-504. doi: 10.1021/jo051558y.

[Figure: see text]. A quantum chemical study has been performed to assess changes in aromaticity along the T1 state Z/E-isomerization pathways of annulenyl-substituted olefins. It is argued that the point on the T1 energy surface with highest substituent aromaticity...

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Kato H, Brink M, Möllerstedt H, et al. Z/E-photoisomerizations of olefins with 4npi- or (4n + 2)pi-electron substituents: zigzag variations in olefin properties along the T(1) state energy surfaces. J Org Chem. 2005;70(23):9495-504doi: 10.1021/jo051558y.
Kato, H., Brink, M., Möllerstedt, H., Piqueras, M. C., Crespo, R., & Ottosson, H. (2005). Z/E-photoisomerizations of olefins with 4npi- or (4n + 2)pi-electron substituents: zigzag variations in olefin properties along the T(1) state energy surfaces. The Journal of organic chemistry, 70(23), 9495-504. https://doi.org/10.1021/jo051558y
Kato, Haruhisa, et al. "Z/E-photoisomerizations of olefins with 4npi- or (4n + 2)pi-electron substituents: zigzag variations in olefin properties along the T(1) state energy surfaces." The Journal of organic chemistry vol. 70,23 (2005): 9495-504. doi: https://doi.org/10.1021/jo051558y
Kato H, Brink M, Möllerstedt H, Piqueras MC, Crespo R, Ottosson H. Z/E-photoisomerizations of olefins with 4npi- or (4n + 2)pi-electron substituents: zigzag variations in olefin properties along the T(1) state energy surfaces. J Org Chem. 2005 Nov 11;70(23):9495-504. doi: 10.1021/jo051558y. PMID: 16268625.
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Influence of excited state aromaticity in the lowest excited singlet states of fulvene derivatives.

Physical chemistry chemical physics : PCCP

Rosenberg M, Ottosson H, Kilså K.
PMID: 21695293
Phys Chem Chem Phys. 2011 Jul 28;13(28):12912-9. doi: 10.1039/c0cp02821e. Epub 2011 Jun 21.

The absorption spectra and excited state dipole moments of four differently substituted fulvenes have been investigated both experimentally and computationally. The results reveal that the excited state dipole moment of fulvenes reverses in the first excited singlet state when...

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Rosenberg M, Ottosson H, Kilså K. Influence of excited state aromaticity in the lowest excited singlet states of fulvene derivatives. Phys Chem Chem Phys. 2011;13(28):12912-9doi: 10.1039/c0cp02821e.
Rosenberg, M., Ottosson, H., & Kilså, K. (2011). Influence of excited state aromaticity in the lowest excited singlet states of fulvene derivatives. Physical chemistry chemical physics : PCCP, 13(28), 12912-9. https://doi.org/10.1039/c0cp02821e
Rosenberg, Martin, et al. "Influence of excited state aromaticity in the lowest excited singlet states of fulvene derivatives." Physical chemistry chemical physics : PCCP vol. 13,28 (2011): 12912-9. doi: https://doi.org/10.1039/c0cp02821e
Rosenberg M, Ottosson H, Kilså K. Influence of excited state aromaticity in the lowest excited singlet states of fulvene derivatives. Phys Chem Chem Phys. 2011 Jul 28;13(28):12912-9. doi: 10.1039/c0cp02821e. Epub 2011 Jun 21. PMID: 21695293.
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DSM-IV and ICD-10 personality disorders: a comparison of a self-report questionnaire (DIP-Q) with a structured interview.

European psychiatry : the journal of the Association of European Psychiatrists

Ottosson H, Bodlund O, Ekselius L, Grann M, von Knorring L, Kullgren G, Lindström E, Söderberg S.
PMID: 19698634
Eur Psychiatry. 1998 Aug;13(5):246-53. doi: 10.1016/S0924-9338(98)80013-8.

OBJECTIVE: Diagnosing personality disorders according to structured expert interviews is time-consuming and costly. For epidemiological studies, self-report instruments have several advantages. The DSM-IV and ICD-10 personality questionnaire (DIP-Q) is a selfreport questionnaire constructed to identify personality disorder according to...

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Ottosson H, Bodlund O, Ekselius L, et al. DSM-IV and ICD-10 personality disorders: a comparison of a self-report questionnaire (DIP-Q) with a structured interview. Eur Psychiatry. 1998;13(5):246-53doi: 10.1016/S0924-9338(98)80013-8.
Ottosson, H., Bodlund, O., Ekselius, L., Grann, M., von Knorring, L., Kullgren, G., Lindström, E., & Söderberg, S. (1998). DSM-IV and ICD-10 personality disorders: a comparison of a self-report questionnaire (DIP-Q) with a structured interview. European psychiatry : the journal of the Association of European Psychiatrists, 13(5), 246-53. https://doi.org/10.1016/S0924-9338(98)80013-8
Ottosson, H, et al. "DSM-IV and ICD-10 personality disorders: a comparison of a self-report questionnaire (DIP-Q) with a structured interview." European psychiatry : the journal of the Association of European Psychiatrists vol. 13,5 (1998): 246-53. doi: https://doi.org/10.1016/S0924-9338(98)80013-8
Ottosson H, Bodlund O, Ekselius L, Grann M, von Knorring L, Kullgren G, Lindström E, Söderberg S. DSM-IV and ICD-10 personality disorders: a comparison of a self-report questionnaire (DIP-Q) with a structured interview. Eur Psychiatry. 1998 Aug;13(5):246-53. doi: 10.1016/S0924-9338(98)80013-8. PMID: 19698634.
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Near sulfur L-edge X-ray absorption spectra of methanethiol in isolation and adsorbed on a Au(111) surface: a theoretical study using the four-component static exchange approximation.

Physical chemistry chemical physics : PCCP

Villaume S, Ekström U, Ottosson H, Norman P.
PMID: 20428572
Phys Chem Chem Phys. 2010 Jun 07;12(21):5596-604. doi: 10.1039/b926109e. Epub 2010 Apr 28.

The relativistic four-component static exchange approach for calculation of near-edge X-ray absorption spectra has been reviewed. Application of the method is made to the Au(111) interface and the adsorption of methanethiol by a study of the near sulfur L-edge...

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Villaume S, Ekström U, Ottosson H, et al. Near sulfur L-edge X-ray absorption spectra of methanethiol in isolation and adsorbed on a Au(111) surface: a theoretical study using the four-component static exchange approximation. Phys Chem Chem Phys. 2010;12(21):5596-604doi: 10.1039/b926109e.
Villaume, S., Ekström, U., Ottosson, H., & Norman, P. (2010). Near sulfur L-edge X-ray absorption spectra of methanethiol in isolation and adsorbed on a Au(111) surface: a theoretical study using the four-component static exchange approximation. Physical chemistry chemical physics : PCCP, 12(21), 5596-604. https://doi.org/10.1039/b926109e
Villaume, Sebastien, et al. "Near sulfur L-edge X-ray absorption spectra of methanethiol in isolation and adsorbed on a Au(111) surface: a theoretical study using the four-component static exchange approximation." Physical chemistry chemical physics : PCCP vol. 12,21 (2010): 5596-604. doi: https://doi.org/10.1039/b926109e
Villaume S, Ekström U, Ottosson H, Norman P. Near sulfur L-edge X-ray absorption spectra of methanethiol in isolation and adsorbed on a Au(111) surface: a theoretical study using the four-component static exchange approximation. Phys Chem Chem Phys. 2010 Jun 07;12(21):5596-604. doi: 10.1039/b926109e. Epub 2010 Apr 28. PMID: 20428572.
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Showing 1 to 12 of 143 entries