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In all cases the sequence of most populated relative orientations, for increasing distances, is found to be identical: The closest distances correspond to face-to-face followed by a dominant role of edge-to-face, while for larger distances the main configuration is edge-to-edge. The corner-to-face configuration plays an almost negligible role. The range of orientational order is also similar, with remnants of orientational correlation discernible up to the fourth solvation shell. The equivalence does not only hold in the qualitative terms just stated but is also quantitative to a large extent once the center-center distance is properly scaled.<\/jats:p>","DOI":"10.1063\/1.3204467","type":"journal-article","created":{"date-parts":[[2009,8,11]],"date-time":"2009-08-11T22:22:55Z","timestamp":1250029375000},"update-policy":"https:\/\/doi.org\/10.1063\/aip-crossmark-policy-page","source":"Crossref","is-referenced-by-count":20,"title":["Is there a common orientational order for the liquid phase of tetrahedral molecules?"],"prefix":"10.1063","volume":"131","author":[{"given":"Rossend","family":"Rey","sequence":"first","affiliation":[{"name":"Universitat Polit\u00e8cnica de Catalunya Departament de F\u00edsica i Enginyeria Nuclear, , Campus Nord B4-B5, Barcelona 08034, Spain"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"317","published-online":{"date-parts":[[2009,8,11]]},"reference":[{"key":"2023062604391388200_c1","doi-asserted-by":"publisher","first-page":"164506","DOI":"10.1063\/1.2720840","volume":"126","year":"2007","journal-title":"J. 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