Relevant bibliographies by topics / Theoretical

Academic literature on the topic 'Theoretical'

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Published: 4 June 2021
Last updated: 30 July 2024

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Journal articles on the topic "Theoretical"

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Išoraite, Margarita. "Rebranding Theoretical Aspects." International Journal of Trend in Scientific Research and Development Volume-2, Issue-5 (August 31, 2018): 2090–93. http://dx.doi.org/10.31142/ijtsrd18254.

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Moskowitz, Clara. "Theoretical Particles, Still Theoretical." Scientific American 312, no. 1 (December 16, 2014): 16. http://dx.doi.org/10.1038/scientificamerican0115-16.

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Leśniewski, Michał Adam, Paweł Dziekański, and Jan Puchała. "INNOVATIVE ENTERPRISE – THEORETICAL PERSPECTIVE." Scientific Notes of Ostroh Academy National University, "Economics" Series 1, no. 24(52) (March 31, 2022): 55–60. http://dx.doi.org/10.25264/2311-5149-2022-24(52)-55-60.

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Innovation is an inseparable element of all human activity in the conditions of the progressing globalization process. In order to develop an enterprise, innovation must be implemented in it, which in turn will result in the emergence of an innovative enterprise. The article presents an innovative enterprise as a concept of development of organizations subject to the influence of globalization processes. A literature study on the subject was used in this study. The study is a discussion on an innovative enterprise. The article is theoretical.
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Matenova, Ayjamal K. "THEORETICAL SIGNIFICANCE OF LINGUISTICS." European International Journal of Multidisciplinary Research and Management Studies 02, no. 10 (October 1, 2022): 31–37. http://dx.doi.org/10.55640/eijmrms-02-10-06.

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This article discusses theoretical significance of linguistics. The initial stage of linguistics is an introduction to linguistics, and it studies the place of language in other phenomena, its structure, and the basic concepts of language science in general. Therefore, this course lays the groundwork for studying and mastering specific language phenomena, vocabulary, phonetic system, grammatical structure on a scientific basis.
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Raghuvanshi, Durgesh. "Data Structure: Theoretical Approach." International Journal of Trend in Scientific Research and Development Volume-3, Issue-1 (December 31, 2018): 268–73. http://dx.doi.org/10.31142/ijtsrd18977.

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Hantsch, Ute, Björn Winkler, Chris J. Pickard, Julian D. Gale, Michele C. Warren, Victor Milman, and Francesco Mauri. "Theoretical investigation of moganite." European Journal of Mineralogy 17, no. 1 (March 3, 2005): 21–30. http://dx.doi.org/10.1127/0935-1221/2005/0017-0021.

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Przhilenskiy, Vladimir. "Theoretical and Post-Theoretical Philosophy." Dialogue and Universalism 27, no. 3 (2017): 125–38. http://dx.doi.org/10.5840/du201727350.

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Firstov, S. A., and T. G. Rogul’. "Theoretical strength and theoretical hardness." Russian Metallurgy (Metally) 2012, no. 10 (October 2012): 837–42. http://dx.doi.org/10.1134/s0036029512100059.

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Fleischer, Isidore. "A Lattice theoretic look at some ring theoretical radicals." Communications in Algebra 20, no. 3 (January 1992): 733–47. http://dx.doi.org/10.1080/00927879208824371.

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Weiner, Bernard. "On theoretical co-existenceversus theoretical integration." European Journal of Psychology of Education 23, no. 4 (December 2008): 433–38. http://dx.doi.org/10.1007/bf03172751.

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Dissertations / Theses on the topic "Theoretical"

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Sudkeaw, Pravit. "Theoretical chemistry." Thesis, University of Canterbury. Chemistry, 1991. http://hdl.handle.net/10092/8785.

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Ab initio Molecular Orbital and Valence-Bond methods and the semiempidcal, AM1 method are applied in the studies of: 1. The proton affinity of diacetylene The gas-phase ion-molecule reaction between diacetylene and a proton was studied theoretically at the MP4SDQ/6-311G** level. The geometries, calculated harmonic vibrational frequencies and the proton affinity of the most stable structures are compared. The results from this study are supported by selected ion flow tube measurements and are compared with other calculations 2. The gas-phase reaction of CH₃CN and CH₃⁺. The reaction between CH₃CN and CH₃⁺ was studied at the MP4SDQ/6-31G* level of theory in order to determine the products and establish the multistep dissociation pathway of the reaction. The location and height of the transition states in the process is used as a criteria for the feasibility of the proposed pathway. The result is compared with the expediential and theoretical studies of the same system done by Wincel and coworkers [146]. 3. The geometries and force constants of small-sized organotin compounds The calculations on 12 small-sized organotin compounds were done at the HF/3- 21G* level of theory. The objective of this study was to provide the force constants of SnX and X-Sn-Y types for the use in Molecular Mechanic calculations of organotin compounds. The calculated geometries and harmonic vibrational frequencies of stannane and methyl stannane are compared with experimental results in order to measure the reliability of the calculations. 4. The chemical properties of CnO, CnO⁺, CnHO⁺, CnS, CnS⁺ and CnHS⁺ species in the instellar clouds CnO and CnS when n = 2 and 3 have been reported to be found in some interstellar clouds. These species in such environments are subjected to ionization and protonation processes. Theoretical studies of these species were done at the MP4SDQ/6-311G** level of theory. The calculations suggest that these species are more stable in protonated forms and could be intermediates of some steady state processes. 5. Theoretical study of C₆H₄+ formation in acetylenic flames C₆H₄⁺ has been detected as an intermediate in acetylenic flames. The semiempirical AM1 method was used to determine the most stable products and to establish a chemical mechanism of the reaction between C₄H₂⁺ and C₂H₂. The results from AM1 method were refined by ab initio calculations at the HF/4-31G andMP4SDQ/6-31G* level. From this study, only chemical pathways involved acyclic structure isomers are feasible. 6. A Valence-Bond study of BH2 radical In this study a Valence-Bond program was used on IBM PC/AT microcomputer to study the correlation between the nuclear bond angle and the angle of hybrid orbitals of BH₂. The energies of BH₂ from the Valence-Bond calculations were also compared with the energies from the Molecular Orbital method at the HF, MP4SDQ and CI level with best orbital energy basis sets, 10s6p/2s1p for boron atom and 6s/1s for hydrogen atoms. GAUSSIAN series programs, the MICROMOL package, the GAMESS program, a Valence-Bond program and the MOPAC program were used to perform the calculations.
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Summe, Lisa Marie. "Theoretical You." Thesis, Virginia Tech, 2016. http://hdl.handle.net/10919/71452.

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Theoretical You is a collection of autobiographical queer love poems told from the perspective of a single speaker. These love poems speak not only to lovers and exes, but also to lust and sex and desire, to the speaker's father (they do not reciprocate the cruelty he has shown her--they are neither malicious nor vindictive), and perhaps most importantly, to the speaker herself--she recognizes herself as a lesbian, as a human, who deserves to love and be loved. While love is the crux of these poems, the collection is just as much about heartbreak (which is, of course, inevitably tied to love, is the consequence of love), heartbreak others have inflicted on the speaker and heartbreak she has inflicted on herself, having walked out on many of the women she addresses in the collection. The poems work to navigate the challenges of heartbreak by confronting homophobia, familial rejection, gender binaries and the appearance norms tied to them, as well as the grief that comes with simply being unable to stop missing someone. Here is a young woman who still loves every woman she has ever been with, who has so much love to give, who has a father who refuses to accept her, in a world that is often cruel. All of this together creates the complicated situation of being perpetually heartbroken, even when the speaker is happily in a relationship, even though she has learned to love herself.
Master of Fine Arts
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Willetts, Andrew. "Theoretical vibrational spectroscopy." Thesis, University of Cambridge, 1990. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.358853.

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Legate, Julie Anne 1972. "Warlpiri : theoretical implications." Thesis, Massachusetts Institute of Technology, 2002. http://hdl.handle.net/1721.1/8152.

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Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Linguistics and Philosophy, 2002.
Includes bibliographical references (v. 2, leaves 230-241).
The issue of non-configurationality is fundamental in determining the possible range of variation in Universal Grammar. This dissertation investigates this issue in the context of Warlpiri, the prototypical non-configurational language. I argue that positing a macroparameter, a single parameter that distinguishes configurational languages from non-configurational, requires variation on a magnitude not permitted by Universal Grammar. After refuting in detail previous macroparametric approaches, I propose a microparametric analysis: non-configurational languages are fully configurational and analysed through fine-grained parameters with independent motivation. I develop this approach for Warlpiri,partially on the basis of new data collected through work with Warlpiri consultants and analysis of Warlpiri texts. Beginning with A-syntax, I show that Warlpiri exhibits short-distance A-scrambling through binding and WCO data. I present an analysis of split ergativity in Warlpiri (ergative-/absolutive case-marking, nominative/accusative agreement), deriving the split from a dissociation of case and agreement, and the inherent nature of ergative case, rather than from non-configurationality. Extending the analysis to applicative constructions in Warlpiri, I identify both symmetric and asymmetric applicatives. I argue that the principled distinctions between them are explained structurally rather than lexically; therefore the applicative data provide evidence for a hierarchical verb phrase in Warlpiri. The analysis reveals the first reported distinction between unaccusative and unergative verbs in the language.
(cont.) Turning to A'-syntax, I argue that word order is not free in Warlpiri; rather Warlpiri displays an articulated left peripheral structure. Thus, word order variations are largely determined by positioning of elements in ordered functional projections based on their status in the discourse. Furthermore, I present evidence from WCO and island effects that elements appear in these projections through movement. Finally, I investigate the wh-scope marking construction, arguing for an indirect dependency approach. In developing the analysis, I argue, contrary to standard assumptions, that the dependent clauses related with verbs of saying in Warlpiri are embedded rather than adjoined. On the basis of a poverty of the stimulus argument, I conclude the construction must follow from independent properties of the language. I propose that it follows from the discontinuous constituent construction, which I equate with split DPs/PPs in Germanic and Slavic languages. The syntactic structure of Warlpiri that emerges from the dissertation strongly supports a configurational analysis of the language, and thereby the microparameter approach to nonconfigurationality.
by Julie Anne Legate.
Ph.D.
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He, Fengxiang. "Theoretical Deep Learning." Thesis, The University of Sydney, 2021. https://hdl.handle.net/2123/25674.

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Deep learning has long been criticised as a black-box model for lacking sound theoretical explanation. During the PhD course, I explore and establish theoretical foundations for deep learning. In this thesis, I present my contributions positioned upon existing literature: (1) analysing the generalizability of the neural networks with residual connections via complexity and capacity-based hypothesis complexity measures; (2) modeling stochastic gradient descent (SGD) by stochastic differential equations (SDEs) and their dynamics, and further characterizing the generalizability of deep learning; (3) understanding the geometrical structures of the loss landscape that drives the trajectories of the dynamic systems, which sheds light in reconciling the over-representation and excellent generalizability of deep learning; and (4) discovering the interplay between generalization, privacy preservation, and adversarial robustness, which have seen rising concerns in deep learning deployment.
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Flores, Francisco J. "Levels of theory and types of theoretical explanation in theoretical physics." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1998. http://www.collectionscanada.ca/obj/s4/f2/dsk3/ftp04/nq31114.pdf.

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Campanera, Alsina Josep Maria. "Theoretical characterisation of metallofullerenes." Doctoral thesis, Universitat Rovira i Virgili, 2005. http://hdl.handle.net/10803/9071.

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INFORME FINAL
"Alguns importants descobriments de la ciència són accidentals. Això fou, certament, el cas del ful·lerè C60. Quan ara fa quatre anys, l'any 2000, vaig iniciar el treball d'investigació sobre els metal·loful·lerens m'havien arribat veus de la importància mediàtica d'aquestes noves estructures però no de la intensa història del seu descobriment. Aquesta m'ha fascinat. Sobretot quan l'any 2003 vaig tenir la possibilitat de fer una estada al grup del professor Kroto de la universitat de Sussex (Gran Bretanya). Llavors els textos, sorprenents però inerts, que havia llegit sobre la història del descobriment dels ful·lerens prenien forma en espais coneguts i personatges propers". Aquest és el prefaci de la meva tesi. Segurament aquesta estada a Sussex al grup d'un dels descobridors dels ful·lerens ha estat el moment més entranyable en aquesta carrera científica per l'estudi dels metal·loful·lerens.
A partir de la síntesi de la molècula de C60 en quantitats apreciables la química dels ful·lerens en general, i en particular amb metalls de transició, ha experimentat un increment espectacular. L'objectiu d'aquesta tesi és l'estudi de l'estructura i la reactivitat de diferents derivats organometàl·lics de ful·lerens o metal·loful·lerens. El treball d'investigació usa les eines de la química computacional (Teoria del funcional de la densitat, DFT) per tal de modelar els metal·loful·lerens més interessants apareguts entre el 1999 i el 2005. Tot i que els metal·loful·lerens presenten una varietat d'estructures formidable, podem classificar-los en tres grans famílies des del punt de vista estructural: un primer grup són els metal·loful·lerens exoèdrics on els metalls es situen fora de la caixa, en un segon grup tenim els metal·loful·lerens heteroèdrics o heteroful·lerens on les caixes de carbonis han estat dopades (certes posicions han estat substituïdes) amb altres elements com ara: N, B, Si, Fe i altres metalls i finalment l'últim grup són els metal·loful·lerens endoèdrics on la derivatització metàl·lica es dóna a l'interior de la caixa. Així l'estudi teòric dels compostos més novedosos i novells de cadascuna de les tres famílies de metal·loful·lerens és el puntal de la present tesi doctoral. Per cadascuna de les famílies hem desgranat l'estructura electrònica i geomètrica, hem descrit el tipus d'enllaç metall-ful·lerè, hem avaluat els factors que intervenen en l'estabilitat relativa dels possibles isòmers, hem també predit la reactivitat davant de reaccions d'addició i finalment els hem caracteritzat des d'un punt de vista físic (càlcul del potencial d'ionització i afinitat electrònica). L'estructura electrònica ens ha permès seleccionar quins metal·loful·lerens endoèdrics seran estables avançant-nos als experimentalistes en la seva cerca de nous complexos. La diversitat de tipologies d'enllaç ha sigut tant gran com famílies de metal·loful·lerens. Hem descrit un enllaç iònic pels metal·loful·lerens endoèdrics, un enllaç covalent en el cas dels metal·loful·lerens heteroèdrics i un enllaç coordinatiu pels metal·loful·lerens exoèdrics. Hem aplicat noves metodologies per l'estudi de l'isomerisme. Les tècniques d'anàlisi multivariant de dades ens han permès esbrinar quins factors són importants per l'estabilitat relativa dels isòmers i a la vegada construir models de predicció per altres isòmers. Així doncs, l'acoblament de la química teòrica i la quimiometria ha estat sens dubte l'aportació més rellevant del present treball d'investigació.

Tarragona, 28 de novembre de 2004
Josep Maria Campanera Alsina


FINAL REPORT

The characterisation of the most novel metallofullerenes up to 2004 has been theoretically and systematically discussed in this study. From the structural point of view, metallofullerenes can be divided into three main groups, all of which have been discussed in this study: endohedral, heterohedral and exohedral metallofullerenes. The main families of compounds studied are Sc3-nMnN@Ck (n = 0-3, M = Y, La; k = 68, 78, 80) (endohedral), CxMn (x = 56, 57, 58, 59; M = Pt, Ir, Os; n = 1, 2) (heterohedral) and (-Ck){M(PH3)2}n (k = 60, 70, 84; M = Pt, Pd, Ni; n = 1, 2, 4, 6) (exohedral). The present study is a step forward in our knowledge of each of these families of compounds, and in particular, in our understanding of the metal-carbon bond, isomerism and reactivity. The DFT method proved to be an excellent computational tool for providing good geometries, for solving the intricacies of the different metal-carbon bonds, for producing experimental data (ionization potentials and electron affinities) and also for making predictions about isomerism stability and reactivity. The principal conclusions drawn about the species studied here are:
Different types of structures, different types of metal-carbon bonds. The metal units in each family of compounds are located differently in relation to the fullerene carbon framework: inside the cage, within the carbon framework and outside the cage. The encapsulation of a trimetallic nitride template unit (TNT, Sc3-nMnN; n = 0-3; M = Y, La) inside the carbon cage to produce TNT endohedral metallofullerenes is explained by an ionic pair (cage-metal) model in which the TNT unit formally transfers six electrons to the cage. On the other hand, in heterohedral metallofullerenes, metals establish a covalent metal-carbon bond without causing oxidation to the metal. Finally, the (MPH3)2 metal units situated exohedrally to the fullerene are only coordinated in a  mode to the CC bond.
Chemometric tools applied to isomerism studies. The regioisomers of heterohedral metallofullerenes are numerous: for example, the stoichiometry C57Pt2 has 47 distinct regioisomers. Thus, chemometric techniques which can manage considerable amounts of data must be used if we want to understand regioisomerism in heterohedral metallofullerenes. These tools have also been very useful for drawing conclusions from the considerable quantities of data provided by the factors which affect the stability of regioisomers. These tools have been used not only for analysing data but also for predicting the stability of other heterofullerenes.
TNT encapsulation stabilizes fullerene isomers that are not available as free fullerenes. TNT endohedral metallofullerenes are formed by the encapsulation of a metallic nitride template inside the following cages: D3-C68:6140, D3h'-C78:5, D5h-C80:6 and Ih-C80:7. Any of these cages have never been detected experimentally.So, endohedral metallofullerenes can make non-classical fullerene isomers available for study. Furthermore, on the basis of the electronic structure we predicted that no other IPR fullerenes between C60 and C84 will be capable of encapsulating a TNT unit, apart from the fullerene isomers that are already known.
Stability of the carbon skeleton is the principal factor that determines the regioisomer stability of the heterofullerenes. Metal atoms occupy neighbouring positions in the most stable structures of C57Pt2 and C56Pt2. Metal substitution deforms the carbon framework and partially destroys the fullerene aromaticity. This is the key factor in determining the stability of these disubstituted clusters. Indeed, it is much easier to make a big hole that permits the incorporation of two Pt atoms in the carbon cage than two smaller holes in two opposite sites of the fullerene.
Prediction of the exohedral reactivity taking into account the full characterization of the different CC bond types. We first performed a full characterization of all CC bond types of the fullerenes Ih-C60:1, D3-C68:6140, D5h-C70:1, D3h'-C78:5, Ih-C80:7, D2-C84:22 and D2d-C84:23. Each CC bond type is characterized by its topology, length, pyramidalization angle and Mayer bond order. This systematization enabled us to identify which sites were most reactive to a nucleophilic addition to free fullerenes or a [4 + 2] cycloaddition to TNT endohedral metallofullerenes.

Tarragona, 8th Novembre 2004
Josep Maria Campanera Alsina
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Ringen, Catherine O. "Vowel harmony theoretical implications /." New York : Garland, 1988. http://catalog.hathitrust.org/api/volumes/oclc/18105466.html.

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Wang, Hao. "Theoretical strength of solids." Diss., Georgia Institute of Technology, 2010. http://hdl.handle.net/1853/42747.

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Theoretical strength of solids is defined as the ultimate strength beyond which plastic deformation, fracture, or decohesion would occur. Understanding the microscopic origin from quantum mechanics and thermoelastic formulation is of great importance to mechanical properties and engineering design of various solids. While quite a few theory models have been made in the past century by several generations of scientists, including Frankel and Born, a general and convincing framework has not been fully established. We study this issue from three respects: (1) Unify various elastic stability criteria for solids that determine an upper bound of theoretical strength; (2) with ab initio method, we test the elastic stability conditions of crystal Au. The phenomenon of bifurcation is observed: under hydrostatic expansion, the rhombohedral modulus reaches zero first of all; while under uniaxial tensile stress, the tetragonal shear modulus first reaches zero; (3) propose a nonlinear theoretical formulation of stability criterion. As an analytic method, this scheme is quite simple, in the mean time, it saves computation resource.
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Patrick, Jane Helen. "Theoretical investigations of ozonolysis." Thesis, Imperial College London, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.271410.

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Books on the topic "Theoretical"

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Kompaneet͡s, A. S. Theoretical physics. Mineola, N.Y: Dover Publications, 2003.

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Stam, Henderikus. Theoretical Psychology. 1 Oliver's Yard, 55 City Road, London EC1Y 1SP United Kingdom: SAGE Publications Ltd, 2012. http://dx.doi.org/10.4135/9781446263648.

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Stahl, Gerry, ed. Theoretical Investigations. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-49157-4.

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Oakley, Jacob G., Michael Butler, Wayne York, Matthew Puckett, and J. Louis Sewell. Theoretical Cybersecurity. Berkeley, CA: Apress, 2022. http://dx.doi.org/10.1007/978-1-4842-8300-4.

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Scheidegger, Adrian E. Theoretical Geomorphology. Berlin, Heidelberg: Springer Berlin Heidelberg, 1991. http://dx.doi.org/10.1007/978-3-642-75659-7.

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Khriplovich, I. B. Theoretical Kaleidoscope. New York, NY: Springer New York, 2008. http://dx.doi.org/10.1007/978-0-387-75252-5.

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Huang, Ji-Ping. Theoretical Thermotics. Singapore: Springer Singapore, 2020. http://dx.doi.org/10.1007/978-981-15-2301-4.

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Honerkamp, Josef, and Hartmann Römer. Theoretical Physics. Berlin, Heidelberg: Springer Berlin Heidelberg, 1993. http://dx.doi.org/10.1007/978-3-642-77984-8.

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Keener, Robert W. Theoretical Statistics. New York, NY: Springer New York, 2010. http://dx.doi.org/10.1007/978-0-387-93839-4.

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Lüdde, Cora S., and Reiner M. Dreizler. Theoretical Mechanics. Berlin, Heidelberg: Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-642-11138-9.

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Book chapters on the topic "Theoretical"

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Saracco, Susanna. "Theoretical Childhood and Theoretical Adulthood." In Plato and Intellectual Development, 53–86. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-52587-7_3.

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Liu, Cheng-Hua. "Theoretical Background." In Springer Theses, 3–21. Singapore: Springer Singapore, 2018. http://dx.doi.org/10.1007/978-981-13-1355-4_2.

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Rao, Jyoti. "Theoretical Framework." In Functionings of Land, 7–37. Singapore: Springer Singapore, 2018. http://dx.doi.org/10.1007/978-981-13-1441-4_2.

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Mehdi, Ali. "Theoretical Framework." In Strategies of Identity Formation, 25–43. Wiesbaden: VS Verlag für Sozialwissenschaften, 2012. http://dx.doi.org/10.1007/978-3-531-18681-8_2.

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Chen, Yuping. "Theoretical Foundations." In Translating Film Subtitles into Chinese, 13–49. Singapore: Springer Singapore, 2019. http://dx.doi.org/10.1007/978-981-13-6108-1_2.

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Tesch, Jan F. "Theoretical Background." In Progress in IS, 19–47. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-319-98723-1_2.

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Amoretti, Andrea. "Theoretical Attempts." In Springer Theses, 29–35. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-61875-3_4.

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Engdahl, Elisabet. "Theoretical Postscript." In Studies in Linguistics and Philosophy, 322–26. Dordrecht: Springer Netherlands, 1986. http://dx.doi.org/10.1007/978-94-009-5323-9_7.

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Miettinen, Kaisa. "Theoretical Background." In Nonlinear Multiobjective Optimization, 37–57. Boston, MA: Springer US, 1998. http://dx.doi.org/10.1007/978-1-4615-5563-6_2.

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Galego Pascual, Javier. "Theoretical Background." In Springer Theses, 29–66. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-48698-3_2.

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Conference papers on the topic "Theoretical"

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GIBSON, B. F. "THEORETICAL PERSPECTIVE." In Proceedings of the International Symposium. WORLD SCIENTIFIC, 2004. http://dx.doi.org/10.1142/9789812702920_0032.

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Vanderhaeghen, Marc. "Theoretical Issues." In SHAPES OF HADRONS. AIP, 2007. http://dx.doi.org/10.1063/1.2734290.

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Forshaw, Jeffrey. "Theoretical summary." In Diffraction 06, International Workshop on Diffraction in High-Energy Physics. Trieste, Italy: Sissa Medialab, 2007. http://dx.doi.org/10.22323/1.035.0023.

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Barducci, Daniele. "Theoretical overview." In Workshop Italiano sulla Fisica  ad Alta Intensità. Trieste, Italy: Sissa Medialab, 2024. http://dx.doi.org/10.22323/1.457.0008.

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GEHRMANN, T. "QCD: THEORETICAL DEVELOPMENTS." In Proceedings of the XXI International Symposium. WORLD SCIENTIFIC, 2004. http://dx.doi.org/10.1142/9789812702975_0007.

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De Santis, Alfredo. "Theoretical Computer Science." In Fifth Italian Conference. WORLD SCIENTIFIC, 1996. http://dx.doi.org/10.1142/9789814531184.

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CHU, C. W. "A Theoretical Alchemist." In In Celebration of the 80th Birthday of C N Yang. WORLD SCIENTIFIC, 2003. http://dx.doi.org/10.1142/9789812791207_0050.

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SPACCAMELA, A. MARCHETTI, P. MENTRASTI, and M. VENTURINI ZILLI. "Theoretical Computer Science." In 4th Italian Conference. WORLD SCIENTIFIC, 1992. http://dx.doi.org/10.1142/9789814536240.

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Degano, Pierpaolo, Ugo Vaccaro, and Giuseppe Pirillo. "Theoretical Computer Science." In Sixth Italian Conference. WORLD SCIENTIFIC, 1998. http://dx.doi.org/10.1142/9789814528023.

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Yamamoto, Kei. "Kaon — Theoretical Overview." In Proceedings of the 3rd J-PARC Symposium (J-PARC2019). Journal of the Physical Society of Japan, 2021. http://dx.doi.org/10.7566/jpscp.33.011104.

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Reports on the topic "Theoretical"

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Cole, Julian D. Theoretical Aerodynamics. Fort Belvoir, VA: Defense Technical Information Center, January 1996. http://dx.doi.org/10.21236/ada304107.

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Kamionkowski, Marc. Theoretical Particle Astrophysics. Office of Scientific and Technical Information (OSTI), August 2013. http://dx.doi.org/10.2172/1089511.

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Vahala, George M. Theoretical Plasma Physics. Office of Scientific and Technical Information (OSTI), December 2013. http://dx.doi.org/10.2172/1247483.

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Kunz, P. D. Theoretical nuclear physics. Office of Scientific and Technical Information (OSTI), October 1990. http://dx.doi.org/10.2172/6472791.

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Author, Not Given. (Theoretical nuclear physics). Office of Scientific and Technical Information (OSTI), January 1991. http://dx.doi.org/10.2172/5219332.

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Gottlieb, S. A. Theoretical particle physics. Office of Scientific and Technical Information (OSTI), May 1990. http://dx.doi.org/10.2172/6191869.

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French, J. B., and D. S. Koltun. Theoretical nuclear physics. Office of Scientific and Technical Information (OSTI), June 1992. http://dx.doi.org/10.2172/7277100.

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Rost, E., and J. R. Shephard. Theoretical nuclear physics. Office of Scientific and Technical Information (OSTI), August 1992. http://dx.doi.org/10.2172/7106073.

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Gottlieb, S. A., A. W. Hendry, V. A. Kostelecky, and D. B. Lichtenberg. Theoretical particle physics. Office of Scientific and Technical Information (OSTI), April 1992. http://dx.doi.org/10.2172/5318356.

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Nedd, Sean. Unorthodox theoretical methods. Office of Scientific and Technical Information (OSTI), January 2012. http://dx.doi.org/10.2172/1048531.

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You might also be interested in the extended bibliographies on the topic 'Theoretical' for particular source types:
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